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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348590Generated: November 3, 2026

(S)-2-tert-Butoxycarbonylamino-3-(2-chloro-6-nitro-phenoxy)-propionic acid benzyl ester → (S)-3-(2-Amino-6-chloro-phenoxy)-2-tert-butoxycarbonylamino-propionic acid

https://huagongshe.com/reaction/1348590

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-tert-Butoxycarbonylamino-3-(2-chloro-6-nitro-phenoxy)-propionic acid benzyl esterHCID 67076911—
CatalystNickelHCID 935—
Product(S)-3-(2-Amino-6-chloro-phenoxy)-2-tert-butoxycarbonylamino-propionic acidHCID 6707675091%

Reaction Steps

In an analogous manner to that described in example 5b), the hydrogenation of (S)-2-tert-butoxycarbonylamino-3-(2-chloro-6-nitro-phenoxy)-propionic acid benzyl ester using Raney-nickel instead of palladium as the catalyst yielded (91%) the title compound as a light brown foam, MS m/e (%): 329.3 (M−H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211573B2
Source datasetuspto-grants-2007_05
ORD IDord-7893781270ce4f2da780c98000c8d4ef
Source noteuspto-grants-2007_05