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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296556Generated: October 30, 2026

Acetate → HCID 131712814, compound

https://huagongshe.com/reaction/2296556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 131712812HCID 131712812—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 131712814HCID 131712814—

Reaction Steps

To a freshly prepared solution of 2,2,2-trichloroethyl 1-hydroxy-2-methylcarbapen-2-em-3-carboxylate in methylene chloride, prepared from 100 mg. (0.317 mmole) of the 1-beta-oxide by Examples 11 and 12) was added 24 microl. (0.317 mmole) of pyridine, 29 microl. (0.317 mmole) of acetic anhydride and 4 mg. of 4-dimethylaminopyridine. Infrared spectral analysis indicated clean conversion to the desired acetate. Following water wash and drying, evaporation to dryness gave 2,2,2-trichloroethyl 1-acetoxy-2-methylcarbapen-2-em-3-carboxylate [ir (CH2Cl2) 1780, 1725, 1700 cm-1 ; Rf 0.7-0.75 (4:1 chloroform:ethyl acetate].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04429128
Source datasetuspto-grants-1984_01
ORD IDord-d5af57b7a8504fa4ba770c82cc04e738
Source noteuspto-grants-1984_01