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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075984Generated: November 1, 2026

Methanol → 2,2,2-Trichloroethyl 2-methoxymethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate

https://huagongshe.com/reaction/1075984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylateHCID 12895262—
CatalystSilver tetrafluoroborateHCID 159722—
SolventDichloromethaneHCID 6344—
Product2,2,2-Trichloroethyl 2-methoxymethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylateHCID 70590443—

Reaction Conditions

Temperature-10 °C

Reaction Steps

2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)-penam-3-carboxylate (1.10 g) was dissolved in methylene chloride (12 ml) and to this solution was added methanol (3 ml). And to the solution was added silver fluoroborate (0.45 g) under stirring under cooling at -10°C and the mixture was stirred for 2 hours at the same temperature. After the reaction was completed, the reaction mixture was filtered and the filtrate was washed with sodium bicarbonate aqueous solution and then with water, dried over magnesium sulfate and thereafter concentrated. The residue was subjected to column chromatography on silica gel (25 g) and eluted with chloroform. The eluate was separated into fractions of about 20 ml and the first and second fractions were collected. After distilling off the solvent, the residue was dried to give oily 2,2,2-trichloroethyl 2-methoxymethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate. Infrared Absorption Spectrum (CHCl3) 3360, 1785, 1757, 1666 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954732
Source datasetuspto-grants-1976_05
ORD IDord-efca60eab76247f699bac04f31c6e52c
Source noteuspto-grants-1976_05