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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976535Generated: October 31, 2026

Pyridine → Methyl N-(oxomethylidene)phenylalaninate

https://huagongshe.com/reaction/1976535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTolueneHCID 1140—
ReactantPhosgeneHCID 6371—
ReactantMethyl L-phenylalaninate hydrochlorideHCID 75736—
SolventDichloromethaneHCID 6344—
ProductMethyl N-(oxomethylidene)phenylalaninateHCID 1514293—

Reaction Conditions

Temperature0 °C

Reaction Steps

A well-stirred cold mixture (0° C.) of phenylalanine methyl ester hydrochloride (200 mg), anhydrous dichloromethane (3 ml), and anhydrous pyridine (295 μl, 4 eq.) was stirred for 15 min. A 2M phosgene solution in toluene (455 μl, 0.98 eq.) was added over 30 sec. followed by stirring for 2 h at 0° C. The reaction mixture was poured into dichloromethane washed with cold IN hydrochloric acid then ice water. Each aqueous layer was back extracted once with dichloromethane. The combined organic layer was washed once with brine, dried over anhydrous magnesium sulfate and concentrated. Distillation under vacuum afforded methyl (S)-2-isocyanato-3-phenylpropanoate (125 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06228842B1
Source datasetuspto-grants-2001_05
ORD IDord-6b54892e9b914fa993a77915ba2e691d
Source noteuspto-grants-2001_05