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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869716Generated: October 29, 2026

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

https://huagongshe.com/reaction/1869716

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 500 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 numberUS07638646B2
Source datasetuspto-grants-2009_12
ORD IDord-5e18d6142a6a4b908bac9be6c3bb98f4
Source noteuspto-grants-2009_12