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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075991Generated: November 2, 2026

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

https://huagongshe.com/reaction/1075991

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 70361197169.9%

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 then 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 (7.8 g). Infrared Absorption Spectrum (Nujol) 3350 ~3400, 1790, 1770 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954732
Source datasetuspto-grants-1976_05
ORD IDord-6818125939774cc6854fc744938dcf23
Source noteuspto-grants-1976_05