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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982739Generated: October 30, 2026

Trifluoroacetic acid → HCID 131714768, compound

https://huagongshe.com/reaction/1982739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 131714767HCID 131714767—
SolventDichloromethaneHCID 6344—
SolventAnisoleHCID 7519—
ProductHCID 131714768HCID 13171476880.1%

Reaction Steps

Trifluoroacetic acid (10 ml) was added to a solution of 7-[2-(2-amino-5-chlorothiazol-4-yl)-2-tert-butoxycarbonylmethoxyiminoacetamido]-3-(1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (2.5 g) in methylene chloride (5.0 ml) and anisole (2.5 ml) under ice-cooling, and then the mixture was stirred for an hour at ambient temperature. The resulting solution was dropwise added to diisopropyl ether (100 ml) and then precipitates were collected by filtration. The precipitates were added to a mixture of water and ethyl acetate, and adjusted to pH 7.5 with 10% aqueous solution of sodium hydroxide. The aqueous layer was separated and adjusted to pH 2.2 with 10% aqueous hydrochloric acid to give the precipitates, which were filtered off and dried over phosphorus pentoxide in vacuo to give 7-[2-(2-amino-5-chlorothiazol-4-yl)-2-carboxymethoxyiminoacetamido]-3-(1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (1.83 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596829
Source datasetuspto-grants-1986_06
ORD IDord-8a6e39ca1a5a46449e4e5234c1a8f3ef
Source noteuspto-grants-1986_06