Production Method 1

624-64-6

590-18-1

89-72-5

Reaction Conditions

1.1 Catalysts: Phenol, 3-methyl-, aluminum salt (3:1) ;  1.5 h, 0.3 MPa, 100 °C
1.2 2.5 h, 180 °C

Reference

Method for preparing ortho-sec-butylphenol from mixed butylene and phenol

, China, , ,

Production Method 2

89-72-5

Reaction Conditions

Reference

Alkylation of phenol with α-methylstyrene, propylene, butenes, isoamylene, 1-octene, and diisobutylene: heterogeneous vs. homogeneous catalysts

Chaudhuri, Basab; Sharma, Man Mohan, Industrial & Engineering Chemistry Research, 1991, 30(1), 227-31

Production Method 3

89-72-5

Reaction Conditions

1.1 Reagents: Phosphoric acid

Reference

Aqueous high-temperature chemistry of carbo- and heterocycles. 10. Aquathermolysis of acyclic and cyclic phenol ethers in the presence of sodium bisulfite or phosphoric acid

Katritzky, Alan R.; Murugan, Ramiah; Balasubramanian, Marudai; Siskin, Michael, Energy & Fuels, 1990, 4(5), 543-6

Production Method 4

89-72-5

Reaction Conditions

Reference

Preparation of o-sec-butylphenol

, USSR, , ,

Production Method 5

9005-53-2

89-72-5

2944-49-2

2082-61-3

1123-94-0

1197-34-8

620-14-4

2039-89-6

3520-52-3

4920-99-4

1074-17-5

3180-09-4

698-71-5

644-35-9

119-64-2

2049-95-8

1321-94-4

1470-94-6

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Palladium ;  1 h, 350 °C; 4 h, 350 °C

Reference

Catalytic hydrotreatment of pyrolytic lignins from different sources to biobased chemicals: Identification of feed-product relations

Figueiredo, M. B.; Deuss, P. J.; Venderbosch, R. H.; Heeres, H. J., Biomass and Bioenergy, 2020, 134,

Production Method 6

89-72-5

Reaction Conditions

1.1 Reagents: Lithium aluminum hydride Solvents: Diethyl ether

Reference

Studies in stereochemistry. XV. Effect of configuration on steric inhibition of resonance in diastereomerically related compounds

Hawthorne, Fred; Cram, Donald J., Journal of the American Chemical Society, 1952, 74, 5859-66

Production Method 7

89-72-5

Reaction Conditions

1.1 Reagents: Sodium hydroxide Solvents: Methanol ,  Water ;  15 min, 85 °C; 85 °C → rt
1.2 Reagents: Hydrochloric acid Solvents: Water ;  neutralized

Reference

A new disposable electrochemical sensor for the individual and simultaneous determination of carbamate pesticides using a nanocomposite modified screen-printed electrode

Kunpatee, Kanjana; Kaewdorn, Kannika; Duangtong, Jatuporn; Chaiyo, Sudkate; Chailapakul, Orawon; et al, Microchemical Journal, 2022, 177,

Production Method 8

89-72-5

Reaction Conditions

1.1 Reagents: Phosphoric acid ;  18 h, 100 °C

Reference

Direct intramolecular C(sp3)-H bond sulfonamidation to synthesize benzosultam derivatives under metal-free conditions

Zhang, He; Sun, Meng-Chan; Yin, Li-Ming; Wei, Donghui; Song, Mao-Ping; et al, Organic Chemistry Frontiers, 2021, 8(24), 6888-6894

Production Method 9

89-72-5

Reaction Conditions

Reference

Investigation of butylphenols by chromatographic and spectral methods

Papazova, D.; Kovacheva, K.; Tsutsulova, A.; Vicheva, G.; Tsvetkova, N., Izvestiya po Khimiya, 1990, 23(1), 128-35

Production Method 10

89-72-5

Reaction Conditions

Reference

o-Alkylphenols

, European Patent Organization, , ,

Production Method 11

89-72-5

Reaction Conditions

Reference

Microbial metabolism of N-methylcarbamate insecticde. I. Metabolism of o-sec-butylphenyl N-methylcarbamate by Aspergillus niger van Tieghem

Suzuki, Takashi; Takeda, Mitsuharu, Chemical & Pharmaceutical Bulletin, 1976, 24(9), 1967-75

2-Sec-Butylphenol Raw materials

• 2-BUTENE
• Lignin
• cis-2-Butene

2-Sec-Butylphenol Preparation Products

• 2-Sec-Butylphenol (89-72-5)
• 2,3-Dimethylanisole (2944-49-2)
• (but-2-en-2-yl)benzene (2082-61-3)
• Phenol,4-ethyl-3-methyl- (1123-94-0)
• Phenol, 3,5-diethyl- (1197-34-8)
• 3-Ethyltoluene (620-14-4)
• 2,5-Dimethylstyrene (stabilized with 4-tert-butylcatechol) (2039-89-6)
• 2-methyl-6-propylphenol (3520-52-3)
• Benzene,1-ethyl-3-(1-methylethyl)- (4920-99-4)
• 1-Methyl-2-propylbenzene (1074-17-5)
• 2-butylphenol (3180-09-4)
• 3-Ethyl-5-methylphenol (698-71-5)
• 2-Propylphenol (644-35-9)
• 1,2,3,4-Tetrahydronaphthalene (119-64-2)
• Tert-Pentylbenzene (2049-95-8)
• Methylnaphthalene (1321-94-4)
• 5-Indanol (1470-94-6)

• 1. An amphipathic trans-acting phosphorothioate RNA element delivers an uncharged phosphorodiamidate morpholino sequence in mdx mouse myotubes?
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• 2. Alternative donor substrates for inverting and retaining glycosyltransferases?
  Luke L. Lairson,Warren W. Wakarchuk Chem. Commun., 2007, 365-367
• 3. An approach towards the synthesis of novel fused nitrogen tricyclic heterocyclic scaffolds via GBB reaction?
  Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
• 4. An artificial photosynthesis system comprising a covalent triazine framework as an electron relay facilitator for photochemical carbon dioxide reduction?
  Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
• 5. An ion-gating multinanochannel system based on a copper-responsive self-cleaving DNAzyme?
  Yang Chen,Di Zhou,Zheyi Meng,Jin Zhai Chem. Commun., 2016,52, 10020-10023

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Phenylpropanes
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

• 5510-99-6(Di-sec-butylphenol, mixture of isomers, predom. 2,6-isomer)
• 74926-87-7(Phenol,4-methyl-2,6-bis(1-methylpropyl)-)
• 26967-67-9(Phenol,(1-methylpropyl)-)
• 1849-18-9(Phenol,2,4-bis(1-methylpropyl)-)
• 74926-93-5(Phenol,2-(1-methylpropyl)-6-propyl-)
• 51528-17-7(Phenol,4-methyl-2-(1-methylpropyl)-)
• 5892-47-7(Phenol,2,4,6-tris(1-methylpropyl)-)
• 74926-97-9(Phenol,2-(1-methylethyl)-6-(1-methylpropyl)-)
• 92625-21-3(Phenol, 4-methyl-2-(1-methyl-2-phenylethyl)-)
• 31291-60-8(Phenol,bis(1-methylpropyl)-)