Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381439Generated: October 29, 2026

Trifluoroacetic acid → HCID 131713194, compound

https://huagongshe.com/reaction/1381439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 131713193HCID 131713193—
SolventDichloromethaneHCID 6344—
ProductHCID 131713194HCID 13171319452.5%

Reaction Steps

To a solution of benzhydryl 7-[2-(2-aminothiazol-4-yl)-2-(2-pyridylmethoxyimino)acetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer) (4.6 g) in methylene chloride (20 ml) and anisole (3.0 g) was added trifluoroacetic acid (11.2 g) under ice-cooling with stirring, and the stirring was continued at ambient temperature for 1.5 hours. The reaction mixture was added dropwise to diisopropyl ether (300 ml) and the precipitated crystals were collected by filtration, followed by suspending in water (70 ml). After adjusting to pH 7.5 with 1N aqueous sodium hydroxide, the resultant aqueous solution was washed with ethyl acetate. The aqueous solution was further adjusted to pH 3.4 with 10% hydrochloric acid, followed by collecting the precipitated crystals to obtain 7-[2-(2-aminothiazol-4-yl)-2-(2-pyridylmethoxyimino)acetamido]-3-vinyl-3-cephem-4-carboxylic acid (syn isomer) (1.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585860
Source datasetuspto-grants-1986_04
ORD IDord-222fd28328034144a814bee787ff4ba6
Source noteuspto-grants-1986_04