Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607942Generated: October 31, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/1607942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 131716123HCID 131716123—
SolventDichloromethaneHCID 6344—
SolventAnisoleHCID 7519—
ProductTrifluoroacetic acidHCID 6422—
ProductHCID 131716122HCID 131716122—

Reaction Steps

To a solution of benzhydryl 7-tert-butoxycarbonylamino-3-(1-methylpyrrolidinio)methyl-3-cephem-4-carboxylate iodide (4.42 g) in a mixture of dichloromethane (12 ml) and anisole (4.4 ml) was added trifluoroacetic acid (8.8 ml) under ice-cooling. After stirring for 30 minutes at room temperature, the reaction mixture was gradually poured into diisopropyl ether. The resultant precipitate was collected by filtration, washed with diisopropyl ether and dried over phosphorus pentoxide to give trifluoroacetic acid salt of 7-amino-3-(1-methyl-1-pyrrolidinio)methyl-3-cephem-4-carboxylic acid iodide (2.51 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868174
Source datasetuspto-grants-1989_09
ORD IDord-2c789edfb4364e48b3593ab801f55639
Source noteuspto-grants-1989_09