(R)-α-allyloxyaminophenylacetic acid benzhydryl ester

Base Information

Chemical Name:(R)-α-allyloxyaminophenylacetic acid benzhydryl ester
CAS No.:494870-83-6
Molecular Formula:C₂₄H₂₃NO₃
Molecular Weight:373.452
Hs Code.:

Synonyms:(R)-α-allyloxyaminophenylacetic acid benzhydryl ester

Suppliers and Price of (R)-α-allyloxyaminophenylacetic acid benzhydryl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (R)-α-allyloxyaminophenylacetic acid benzhydryl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-α-allyloxyaminophenylacetic acid benzhydryl ester

There total 3 articles about (R)-α-allyloxyaminophenylacetic acid benzhydryl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 6542-54-7
O-Allylhydroxylamine

: 130605-58-2
(S)-α-allyloxyaminophenylacetic acid benzhydryl ester

: 494870-83-6
(R)-α-allyloxyaminophenylacetic acid benzhydryl ester

Guidance literature:: (S)-α-allyloxyaminophenylacetic acid benzhydryl ester; With 2,6-dimethylpyridine; trifluoromethylsulfonic anhydride; In dichloromethane; at -68 ℃; for 1h;

O-Allylhydroxylamine; In dichloromethane; at 20 ℃; for 17h;
DOI:10.1139/v04-174

Reference yield:

: 17199-29-0
(S)-Mandelic acid

: 494870-83-6
(R)-α-allyloxyaminophenylacetic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 80 percent / ethyl acetate / 1 h / 20 °C

2.1: triflic anhydride; 2,6-lutidine / CH₂Cl₂ / 1 h / -68 °C

2.2: CH₂Cl₂ / 17 h / 20 °C

With 2,6-dimethylpyridine; trifluoromethylsulfonic anhydride; In dichloromethane; ethyl acetate;
DOI:10.1139/v04-174

Reference yield:

: 908093-98-1
diazodiphenylmethane

: 494870-83-6
(R)-α-allyloxyaminophenylacetic acid benzhydryl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 80 percent / ethyl acetate / 1 h / 20 °C

2.1: triflic anhydride; 2,6-lutidine / CH₂Cl₂ / 1 h / -68 °C

2.2: CH₂Cl₂ / 17 h / 20 °C

With 2,6-dimethylpyridine; trifluoromethylsulfonic anhydride; In dichloromethane; ethyl acetate;
DOI:10.1139/v04-174