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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603246Generated: October 31, 2026

Triethylamine → HCID 13124491, compound

https://huagongshe.com/reaction/1603246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl chloroformateHCID 10928—
ReactantBenzyloxycarbonyl-L-phenylalanineHCID 70878—
SolventChloroformHCID 6212—
ProductHCID 13124491HCID 13124491—
ProductHCID 15428308HCID 15428308—

Reaction Conditions

Temperature-2.5 °C

Reaction Steps

To a solution of N-benzyloxycarbonyl-L-phenylalanine (5.98 g, 20 mmol) and triethylamine (2.02 g, 20 mmol) in chloroform (100 ml), ethyl chloroformate (2.18 g, 20 mmol) was added at -15° C. The reaction mixture was stirred at a bath temperature of -10 to 5° C. for 1.5 hrs. Then a precooled (ca. -15° C.) solution of (3S,4S)-3-amino-4-acetoxy-azetidin-2-one in ethyl acetate, which was obtained from hydrogenation of (3S,4S)-3-benzyloxycarbonylamino-4-acetoxy-azetidin-2-one (see above), was added at -15° C. and stirring was continued at a bath temperature of -15 to 5° C. for 1 hr. After removal of solvent, the residue was dissolved in ethyl acetate, washed with water, brine and dried over sodium sulfate. After removal of solvent, the residue was purified by silica gel column chromatography using hexane-ethyl acetate (1:2) as eluent and the title compound was obtained as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05986108
Source datasetuspto-grants-1999_11
ORD IDord-f684e75ecec0442183ea2b4d7b4c9984
Source noteuspto-grants-1999_11