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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811681Generated: November 4, 2026

Hydrochloric Acid → (alphaR)-alpha-((Methoxycarbonyl)amino)benzeneacetic acid

https://huagongshe.com/reaction/1811681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl chloroformateHCID 6586—
ReactantPhenylglycine, D-HCID 70134—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(alphaR)-alpha-((Methoxycarbonyl)amino)benzeneacetic acidHCID 1091077580%

Reaction Steps

D-(−)-α-Phenylglycine (0.165 mmol) was dissolved in tetrahydrofuran (500 mL), followed by the addition of NaHCO3 (0.496 mmol) in water (500 mL), and then the addition of methylchloroformate (0.182 mmol) at room temperature. The reaction mixture was stirred at room temperature overnight. The mixture was acidified to pH=3 with HCl (1N) and the volatile was concentrated in vacuo. The aqueous layer was extracted with ethyl acetate and the organic layer was dried over MgSO4, filtered, and concentrated in vacuo to give compound 31 as a pale yellow solid in 80% yield. MS (ESI, EI+) m/z=209 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362068B2
Source datasetuspto-grants-2013_01
ORD IDord-1e64875974884549b37b75b1f183f1f7
Source noteuspto-grants-2013_01