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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650924Generated: November 3, 2026

Trifluoroacetic acid → HCID 131713437, compound

https://huagongshe.com/reaction/1650924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 131713438HCID 131713438—
SolventDichloromethaneHCID 6344—
SolventAnisoleHCID 7519—
ProductHCID 131713437HCID 13171343768%

Reaction Steps

Trifluoroacetic acid (9.2 ml) was added to a suspension of 7-[2-(2-amino-5-chlorothiazol-4-yl)-2-t-butoxycarbonylmethoxyiminoacetamido]-3-methyl-3-cephem-4-carboxylic acid (syn isomer) (2.3 g) in dichloromethane (5 ml) and anisole (2.3 ml) at ambient temperature and the mixture was stirred for 1.5 hours at same temperature. To the resulting solution was added the isopropyl ether and stirred. The precipitates were collected by filtration, washed with isopropyl ether. The precipitates were added to a mixture of ethyl acetate and water, and adjusted to pH 7.5 with saturated aqueous sodium bicarbonate. The separated aqueous layer was adjusted to pH 2.2 with 10% hydrochloric acid under ice cooling. The precipitates were filtered off, washed with ice water and dried over phosphorus pentoxide in vacuo to give 7-[2-(2-amino-5-chlorothiazol-4-yl)-2-carboxymethoxyiminoacetamido]-3-methyl-3-cephem-4-carboxylic acid (syn isomer) (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925948
Source datasetuspto-grants-1990_05
ORD IDord-0e03f432ff3741e7a0f99caec8122492
Source noteuspto-grants-1990_05