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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856177Generated: November 2, 2026

Methanol → 2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-aminopenam-3-carboxylate hydrochloride

https://huagongshe.com/reaction/1856177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylateHCID 12895262—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-aminopenam-3-carboxylate hydrochlorideHCID 70361197159%

Reaction Conditions

Temperature-15 °C

Reaction Steps

2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate (10.8 g) was dissolved in dried methylene chloride (300 ml). To this solution were added under cooling at -35° C. dried dimethylaniline (3.6 g) and the phosphorus pentachloride (6.4 g) and the mixture was stirred for 2.5 hours at the same temperature. To the solution was added dropwise anhydrous methanol (6.4 g) at the same temperature and the mixture was stirred for 1 hour at -15° C. Water (6.5 ml) was added to the solution and the solution was vigorously stirred for 30 minutes. After the reaction, precipitates were collected by filtration, washed with methylene chloride and further with ether and then dried to give powdery 2,2,2-trichloroethyl 2-bromomethyl-2-methyl-6-aminopenam-3-carboxylate hydrochloride (7.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04218374
Source datasetuspto-grants-1980_08
ORD IDord-7a30611ae15a4575949a8e4ce645d67c
Source noteuspto-grants-1980_08