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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648377Generated: November 1, 2026

Ethyl chloroformate → EtOCO-D,L-Phe(alphaMe)-OH

https://huagongshe.com/reaction/1648377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantDiisopropylethylamineHCID 81531—
ReactantDL-alpha-MethylphenylalanineHCID 108055—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEtOCO-D,L-Phe(alphaMe)-OHHCID 2019275798%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring suspension of D,L-Phe(αMe)-OH (7.5 g, 42 mmol) in tetrahydrofuran (250 mL) was added N,O-bis(trimethylsilyl)acetamide (12.8 g, 62.8 mmol). Upon clarification the solution was cooled to 0° C. and N,N-diisopropylethylamine (5.4 g, 42 mmol) was added, followed by ethyl chloroformate (4.5 g, 42 mmol). After 2 h, water (100 mL) was added and then the organic solvent was removed in vacuo. The aqueous phase was diluted with 1N NaOH and washed twice with diethyl ether. The aqueous phase was then acidified to pH 2 with concentrated HCl and extracted three times with ethyl acetate. The combined ethyl acetate extracts were dried (Na2SO4), filtered and concentrated in vacuo to give 10.3 g (98% yield) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436229
Source datasetuspto-grants-1995_07
ORD IDord-7656687a574b4fa383524df790d8c9f3
Source noteuspto-grants-1995_07