Production Method 1

80466-51-9

Reaction Conditions

1.1 Reagents: Thiophenol Solvents: Acetic acid ,  Methanol ;  4.5 h, rt

Reference

Cyclic sulfamidite as simultaneous protecting group for amino alcohols: development of a mild deprotection protocol using thiophenol

Sakata, Juri; et al, Chemical & Pharmaceutical Bulletin, 2020, 68(10), 996-1000

Production Method 2

2854-16-2

100-52-7

80466-51-9

Reaction Conditions

Reference

Pterins. VII. Preparation of 6,6-dimethyl-5,6,7,8-tetrahydropterin hydrochloride

Armarego, Wilfred L. F.; et al, Australian Journal of Chemistry, 1981, 34(9), 1921-33

Production Method 3

2854-16-2

100-52-7

80466-51-9

Reaction Conditions

1.1 Solvents: Ethanol ;  3 h, rt
1.2 Reagents: Sodium borohydride ;  0 °C; overnight, 0 °C → rt

Reference

Zinc-Catalyzed Esterification of N-β-Hydroxyethylamides: Removal of Directing Groups under Mild Conditions

Nishii, Yuji; et al, European Journal of Organic Chemistry, 2017, 2017(34), 5010-5014

Production Method 4

558-30-5

80466-51-9

Reaction Conditions

1.1 Solvents: Methanol ;  overnight, 100 °C

Reference

2-(2-Oxo-morpholin-3-yl)-acetamide Derivatives as Broad-Spectrum Antifungal Agents

Bardiot, Dorothee; et al, Journal of Medicinal Chemistry, 2015, 58(3), 1502-1512

Production Method 5

558-30-5

80466-51-9

Reaction Conditions

1.1 Catalysts: Dabco Solvents: Water ;  12 h, rt

Reference

Thermal Safety and Structure-Related Reactivity Investigation of Five-Membered Cyclic Sulfamidates

Ferrari, Thomas ; et al, Organic Process Research & Development, 2022, 26(9), 2614-2623

Production Method 6

52853-55-1

80466-51-9

Reaction Conditions

1.1 Reagents: Phosphoric acid ,  Sulfuric acid Solvents: Water ;  2 h, 20 - 25 °C
1.2 Reagents: Sodium hydroxide Solvents: Water ;  basified, 0 °C

Reference

Synthesis and Anti-Monoamine Oxidase Activity of 2-Substituted 4,4-Dimethyl-1,2,3,4-tetrahydroisoquinoline Derivatives

Aghekyan, A. A.; et al, Russian Journal of Organic Chemistry, 2022, 58(10), 1409-1415

Production Method 7

80466-51-9

Reaction Conditions

1.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ;  26 - 28 °C; overnight, 26 - 28 °C
2.1 Reagents: Phosphoric acid ,  Sulfuric acid Solvents: Water ;  2 h, 20 - 25 °C
2.2 Reagents: Sodium hydroxide Solvents: Water ;  basified, 0 °C

Reference

Synthesis and Anti-Monoamine Oxidase Activity of 2-Substituted 4,4-Dimethyl-1,2,3,4-tetrahydroisoquinoline Derivatives

Aghekyan, A. A.; et al, Russian Journal of Organic Chemistry, 2022, 58(10), 1409-1415

1-(Benzylamino)-2-methylpropan-2-OL Raw materials

• 1,1-Dimethyloxirane
• 1-Amino-2-methylpropan-2-ol
• N-benzyl-2-methyl-2-propen-1-amine hydrochloride
• Benzaldehyde

1-(Benzylamino)-2-methylpropan-2-OL Preparation Products

• 1-(Benzylamino)-2-methylpropan-2-OL (80466-51-9)

• 1. An amphoteric reactivity of a mixed-valent bis(μ-oxo)dimanganese(iii,iv) complex acting as an electrophile and a nucleophile?
  Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
• 2. An atomic scale study of defects in Co2FeAl
  Ravi Kumar Yadav,R. Govindaraj Phys. Chem. Chem. Phys., 2020,22, 26876-26886
• 3. An artificial CO-releasing metalloprotein built by histidine-selective metallation?
  Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
• 4. Alumina coating on 5 V lithium cobalt fluorophosphate cathode material for lithium secondary batteries – synthesis and electrochemical properties?
  S. Amaresh,K. Karthikeyan,K. J. Kim,Y. S. Lee RSC Adv., 2014,4, 23107-23115
• 5. An automatic determination of thoria in thoria-urania mixtures
  Analyst, 1966,91, 208-210

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Phenylmethylamines

• 27159-32-6(1-(Benzylamino)propan-2-ol)
• 93723-61-6(2-Propanol,1-[bis(phenylmethyl)amino]-)
• 428855-18-9(Cyclopropanol, 1-[[(phenylmethyl)amino]methyl]-)
• 344868-41-3(1-(Dibenzylamino)-2-methyl-2-propanol)
• 91339-81-0(2-Propanol,1-[methyl(phenylmethyl)amino]-)
• 428855-17-8(1-[(dibenzylamino)methyl]cyclopropan-1-ol)
• 869882-24-6(2-Propanol, 1,1'-[(phenylmethyl)imino]bis[2-methyl-)
• 113133-53-2(2-Propanol, 2-methyl-1-[methyl(phenylmethyl)amino]-)
• 162240-94-0(2-Propanol, 1-[(phenylmethyl)amino]-, (2R)-)
• 865604-12-2(2-PROPANOL, 1,1'-[1,4-PHENYLENEBIS(METHYLENEIMINO)]BIS-)