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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23217Generated: October 27, 2026

Hydrochloric Acid → Methyl (2S)-2-amino-3-(3,5-difluorophenyl)propanoate

https://huagongshe.com/reaction/23217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant(2S)-2-[(tert-Butoxycarbonyl)amino]-3-(3,5-difluorophenyl)propionic acid methyl esterHCID 9836527—
ReactantMethyl (2S)-2-[[(benzyloxy)carbonyl]amino]-3-(3,5-difluorophenyl)propanoateHCID 9968214—
SolventMethanolHCID 887—
ProductMethyl (2S)-2-amino-3-(3,5-difluorophenyl)propanoateHCID 9920793—

Reaction Steps

(2S)-2-[(tert-butoxycarbonyl)amino]-3-(3,5-difluorophenyl)propanoic acid methyl ester (II, EXAMPLE 1, 0.60 g (0.002 moles, 1 equivalent), methanol (20 mL) and hydrochloric acid (3N, 20 mL) are mixed. The mixture is then heated to 50° and stirred until complete as measured by HPLC. When the reaction is complete, the contents are cooled to 20-25° and the pH of the mixture is adjusted to 8 with saturated sodium bicarbonate and then concentrated under reduced pressure. This mixture is extracted with ethyl acetate (2×20 mL) and the combined organic phases are dried over sodium sulfate, filtered and concentrated, HPLC (Retention time=2.89 min; Zorbax RX-C8 acetonitrile/0.05M potassium dihydrogen phosphate, 60/40; 1.0 mL/min, λ=210 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849750B2
Source datasetuspto-grants-2005_02
ORD IDord-1f4cdcf0cc974bdca7f442940b6aaf69
Source noteuspto-grants-2005_02