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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58798Generated: October 29, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/58798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-methoxypyridin-4-yl)propanoateHCID 86681449—
SolventDichloromethaneHCID 6344—
ProductTrifluoroacetic acidHCID 6422—
Product(S)-methyl 2-amino-3-(2-methoxypyridin-4-yl)propanoateHCID 117608201—

Reaction Steps

TFA (5 mL) was added to a solution of (S)-methyl 2-(tert-butoxycarbonylamino)-3-(2-methoxypyridin-4-yl)propanoate (2.4 g, 7.7 mmol) in CH2Cl2 (10 mL) at 0° C. with stirring. The mixture was stirred for 1 h and then concentrated to dryness. The residue was azeotroped three times with EtOAc (10 mL for each portion) to remove residual TFA to afford crude (S)-methyl 2-amino-3-(2-methoxypyridin-4-yl)propanoate as its TFA salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434761B2
Source datasetuspto-grants-2016_09
ORD IDord-bf12afae3461471e9db3f5d4a111db16
Source noteuspto-grants-2016_09