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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083163Generated: November 2, 2026

Tetrahydrofuran → 2,2,2-Trichloroethyl 3-methyl-3-methoxy-7-(2-phenylacetamido)-cepham-4-carboxylate

https://huagongshe.com/reaction/2083163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylateHCID 12895262—
CatalystSilver tetrafluoroborateHCID 159722—
SolventMethanolHCID 887—
Product2,2,2-Trichloroethyl 3-methyl-3-methoxy-7-(2-phenylacetamido)-cepham-4-carboxylateHCID 70590775—

Reaction Steps

2,2,2-Trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate (0.55 g) was dissolved in a mixture of tetrahydrofuran (5 ml) and methanol (5 ml). To this solution was added silver fluoroborate (0.24 g) under cooling and then the mixture was stirred for 1 hour. The reaction mixture was concentrated and the obtained residue was dissolved in chloroform. This solution was washed with a saturated sodium bicarbonate aqueous solution and with water and dried over magnesium sulfate. The residue obtained by distilling off the solvent was subjected to chromatography on silica gel using chloroform as developing solvent. The obtained crystals were recrystallized from carbon tetrachloride to give 2,2,2-trichloroethyl 3-methyl-3-methoxy-7-(2-phenylacetamido)-cepham-4-carboxylate (0.27 g), mp. 132° to 133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04084049
Source datasetuspto-grants-1978_04
ORD IDord-88960ef157bb4e1b9b526653f44a6022
Source noteuspto-grants-1978_04