(2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID

Base Information

Chemical Name:(2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID
CAS No.:109971-52-0
Molecular Formula:C₉H₁₀ClNO₃
Molecular Weight:215.636
Hs Code.:
Mol file:109971-52-0.mol

Synonyms:(2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID;(R)-2-amino-2-(3-chloro-4-methoxyphenyl)acetic acid

Suppliers and Price of (2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID

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 3 raw suppliers

Chemical Property of (2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID

Chemical Property:

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID

There total 5 articles about (2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID 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:

: 185342-14-7
(R)-Azido-(3-chloro-4-methoxy-phenyl)-acetic acid

: 109971-52-0,53091-63-7
(R)-Amino-(3-chloro-4-methoxy-phenyl)-acetic acid

Guidance literature:: With hydrogenchloride; hydrogen; palladium on activated charcoal; In ethyl acetate;
DOI:10.1016/S0040-4039(00)00030-7

Reference yield:

: 13721-20-5
2-(3-chloro-4-methoxyphenyl)acetic acid

: 109971-52-0,53091-63-7
(R)-Amino-(3-chloro-4-methoxy-phenyl)-acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: Et₃N

2: tetrahydrofuran / -78 - 20 °C

3: KHMDS; Trisyl-N₃ / acetic acid / Heating

4: LiOH / tetrahydrofuran; H₂O / 0 °C

5: H₂; HCl / Pd-C / ethyl acetate

With hydrogenchloride; lithium hydroxide; 2,4,6-Triisopropylbenzenesulfonyl azide; hydrogen; potassium hexamethylsilazane; triethylamine; palladium on activated charcoal; In tetrahydrofuran; water; acetic acid; ethyl acetate; 1: Acylation / 2: Substitution / 3: Evans asymmetric azidation / 4: Hydrolysis / 5: Catalytic hydrogenation;
DOI:10.1016/S0040-4039(00)00030-7

Reference yield:

: 185342-17-0
(4R,5S)-3-[2-(3-Chloro-4-methoxy-phenyl)-acetyl]-4-methyl-5-phenyl-oxazolidin-2-one

: 109971-52-0,53091-63-7
(R)-Amino-(3-chloro-4-methoxy-phenyl)-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: KHMDS; Trisyl-N₃ / acetic acid / Heating

2: LiOH / tetrahydrofuran; H₂O / 0 °C

3: H₂; HCl / Pd-C / ethyl acetate

With hydrogenchloride; lithium hydroxide; 2,4,6-Triisopropylbenzenesulfonyl azide; hydrogen; potassium hexamethylsilazane; palladium on activated charcoal; In tetrahydrofuran; water; acetic acid; ethyl acetate; 1: Evans asymmetric azidation / 2: Hydrolysis / 3: Catalytic hydrogenation;
DOI:10.1016/S0040-4039(00)00030-7