Cas no 82815-86-9 (ethyl 2-(3-methoxyphenoxy)acetate)

ethyl 2-(3-methoxyphenoxy)acetate structure
82815-86-9 structure
Product Name:ethyl 2-(3-methoxyphenoxy)acetate
CAS No:82815-86-9
MF:C11H14O4
MW:210.226463794708
MDL:MFCD01162395
CID:708599
Update Time:2024-01-23

ethyl 2-(3-methoxyphenoxy)acetate Chemical and Physical Properties

Names and Identifiers

    • Acetic acid,2-(3-methoxyphenoxy)-, ethyl ester
    • (3-METHOXYPHENOXY) ACETIC ACID ETHYL ESTER
    • ethyl (3-methoxyphenoxy)acetate
    • ethyl 2-(3-methoxyphenoxy)acetate
    • ethyl m-methoxyphenoxyacetate
    • Resorcin-methylaether-O-essigsaeure-aethylester
    • Acetic acid, (3-methoxyphenoxy)-, ethyl ester (9CI)
    • Acetic acid, (m-methoxyphenoxy)-, ethyl ester (6CI, 7CI)
    • Ethyl 2-(3-methoxyphenoxy)acetate (ACI)
    • 3-Methoxyphenoxyacetic acid ethyl ester
    • MDL： MFCD01162395
    • Inchi： 1S/C11H14O4/c1-3-14-11(12)8-15-10-6-4-5-9(7-10)13-2/h4-7H,3,8H2,1-2H3
    • InChI Key： RGCXMLIHLKQOHN-UHFFFAOYSA-N
    • SMILES： O=C(COC1C=C(OC)C=CC=1)OCC

Computed Properties

  • Exact Mass: 210.08900

Experimental Properties

  • PSA: 44.76000
  • LogP: 1.63710

ethyl 2-(3-methoxyphenoxy)acetate Customs Data

  • HS CODE：2918990090
  • Customs Data：

    China Customs Code:

    2918990090

    Overview:

    2918990090. Other additional oxy carboxylic acids(Including anhydrides\Acyl halide\Peroxides, peroxyacids and derivatives of this tax number). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

ethyl 2-(3-methoxyphenoxy)acetate Pricemore >>

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TRC
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SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
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ethyl 2-(3-methoxyphenoxy)acetate Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Acetone ;  30 min, rt → reflux
1.2 5 min, reflux; 12 h, reflux
Reference
Transition-metal-free conversion of lignin model compounds to high-value aromatics: scope and chemoselectivity
Lee, Tae Woo; et al, Green Chemistry, 2018, 20(16), 3761-3771

Production Method 2

Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ;  overnight, 70 °C
Reference
Design and synthesis of α-phenoxy-N-sulfonylphenyl acetamides as Trypanosoma brucei Leucyl-tRNA synthetase inhibitors
Xin, Weixiang; et al, European Journal of Medicinal Chemistry, 2020, 185,

Production Method 3

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ;  20 min, 0 °C; 3 h, 0 °C → 60 °C; 60 °C → 0 °C
1.2 Reagents: Sodium sulfate decahydrate ;  0 °C; 15 min, rt
2.1 Reagents: Sodium tert-butoxide ,  Oxygen Solvents: tert-Butanol ;  16 h, 1 atm, 30 °C
2.2 Reagents: Water
2.3 Reagents: Hydrochloric acid Solvents: Water ;  pH 1
3.1 Reagents: Potassium carbonate Solvents: Acetone ;  30 min, rt → reflux
3.2 5 min, reflux; 12 h, reflux
Reference
Transition-metal-free conversion of lignin model compounds to high-value aromatics: scope and chemoselectivity
Lee, Tae Woo; et al, Green Chemistry, 2018, 20(16), 3761-3771

Production Method 4

Reaction Conditions
1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Acetone ,  Water ;  rt → 63 °C
1.2 Solvents: Acetone ;  1 h, 63 °C; 7 h, 63 °C; 63 °C → rt; 13 h, rt
Reference
Development of a Robust Protocol for the Synthesis of 6-Hydroxybenzofuran-3-carboxylic Acid
Gallou, Isabelle; et al, Organic Process Research & Development, 2020, 24(5), 861-866

Production Method 5

Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Acetone ;  rt; 24 h, reflux
Reference
Palladium-Catalyzed Carbonylative Cyclization of Aryl Alkenes/Alkenols: A New Reaction Mode for the Synthesis of Electron-Rich Chromanes
Li, Shuang; et al, Organic Letters, 2015, 17(5), 1240-1243

Production Method 6

Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Acetonitrile ;  5 h, reflux
Reference
Expedient discovery for novel antifungal leads: 1,3,4-Oxadiazole derivatives bearing a quinazolin-4(3H)-one fragment
Wang, Xiaobin; et al, Bioorganic & Medicinal Chemistry, 2021, 45,

Production Method 7

Reaction Conditions
1.1 Reagents: Sodium tert-butoxide ,  Oxygen Solvents: tert-Butanol ;  16 h, 1 atm, 30 °C
1.2 Reagents: Water
1.3 Reagents: Hydrochloric acid Solvents: Water ;  pH 1
2.1 Reagents: Potassium carbonate Solvents: Acetone ;  30 min, rt → reflux
2.2 5 min, reflux; 12 h, reflux
Reference
Transition-metal-free conversion of lignin model compounds to high-value aromatics: scope and chemoselectivity
Lee, Tae Woo; et al, Green Chemistry, 2018, 20(16), 3761-3771

Production Method 8

Reaction Conditions
1.1 Reagents: Sodium tert-butoxide ,  Oxygen Solvents: tert-Butanol ;  16 h, 1 atm, 30 °C
1.2 Reagents: Water
1.3 Reagents: Hydrochloric acid Solvents: Water ;  pH 1
2.1 Reagents: Potassium carbonate Solvents: Acetone ;  30 min, rt → reflux
2.2 5 min, reflux; 12 h, reflux
Reference
Transition-metal-free conversion of lignin model compounds to high-value aromatics: scope and chemoselectivity
Lee, Tae Woo; et al, Green Chemistry, 2018, 20(16), 3761-3771

Production Method 9

Reaction Conditions
1.1 Reagents: Sodium tert-butoxide ,  Oxygen Solvents: tert-Butanol ;  16 h, 1 atm, 30 °C
1.2 Reagents: Water
1.3 Reagents: Hydrochloric acid Solvents: Water ;  pH 1
2.1 Reagents: Potassium carbonate Solvents: Acetone ;  30 min, rt → reflux
2.2 5 min, reflux; 12 h, reflux
Reference
Transition-metal-free conversion of lignin model compounds to high-value aromatics: scope and chemoselectivity
Lee, Tae Woo; et al, Green Chemistry, 2018, 20(16), 3761-3771

Production Method 10

Reaction Conditions
1.1 Reagents: Sodium tert-butoxide ,  Oxygen Solvents: tert-Butanol ;  16 h, 1 atm, 30 °C
1.2 Reagents: Water
1.3 Reagents: Hydrochloric acid Solvents: Water ;  pH 1
2.1 Reagents: Potassium carbonate Solvents: Acetone ;  30 min, rt → reflux
2.2 5 min, reflux; 12 h, reflux
Reference
Transition-metal-free conversion of lignin model compounds to high-value aromatics: scope and chemoselectivity
Lee, Tae Woo; et al, Green Chemistry, 2018, 20(16), 3761-3771

Production Method 11

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ;  20 min, 0 °C; 3 h, 0 °C → 60 °C; 60 °C → 0 °C
1.2 Reagents: Sodium sulfate decahydrate ;  0 °C; 15 min, rt
2.1 Reagents: Sodium tert-butoxide ,  Oxygen Solvents: tert-Butanol ;  16 h, 1 atm, 30 °C
2.2 Reagents: Water
2.3 Reagents: Hydrochloric acid Solvents: Water ;  pH 1
3.1 Reagents: Potassium carbonate Solvents: Acetone ;  30 min, rt → reflux
3.2 5 min, reflux; 12 h, reflux
Reference
Transition-metal-free conversion of lignin model compounds to high-value aromatics: scope and chemoselectivity
Lee, Tae Woo; et al, Green Chemistry, 2018, 20(16), 3761-3771

Production Method 12

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ;  20 min, 0 °C; 3 h, 0 °C → 60 °C; 60 °C → 0 °C
1.2 Reagents: Sodium sulfate decahydrate ;  0 °C; 15 min, rt
2.1 Reagents: Sodium tert-butoxide ,  Oxygen Solvents: tert-Butanol ;  16 h, 1 atm, 30 °C
2.2 Reagents: Water
2.3 Reagents: Hydrochloric acid Solvents: Water ;  pH 1
3.1 Reagents: Potassium carbonate Solvents: Acetone ;  30 min, rt → reflux
3.2 5 min, reflux; 12 h, reflux
Reference
Transition-metal-free conversion of lignin model compounds to high-value aromatics: scope and chemoselectivity
Lee, Tae Woo; et al, Green Chemistry, 2018, 20(16), 3761-3771

Production Method 13

Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ;  20 min, 0 °C; 3 h, 0 °C → 60 °C; 60 °C → 0 °C
1.2 Reagents: Sodium sulfate decahydrate ;  0 °C; 15 min, rt
2.1 Reagents: Sodium tert-butoxide ,  Oxygen Solvents: tert-Butanol ;  16 h, 1 atm, 30 °C
2.2 Reagents: Water
2.3 Reagents: Hydrochloric acid Solvents: Water ;  pH 1
3.1 Reagents: Potassium carbonate Solvents: Acetone ;  30 min, rt → reflux
3.2 5 min, reflux; 12 h, reflux
Reference
Transition-metal-free conversion of lignin model compounds to high-value aromatics: scope and chemoselectivity
Lee, Tae Woo; et al, Green Chemistry, 2018, 20(16), 3761-3771

ethyl 2-(3-methoxyphenoxy)acetate Raw materials

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