Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052179Generated: November 3, 2026

Trifluoroacetate → HCID 70352943, compound

https://huagongshe.com/reaction/2052179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetateHCID 84468—
ReactantHCID 70582096HCID 70582096—
SolventAnisoleHCID 7519—
ProductHCID 70352943HCID 7035294373.8%

Reaction Steps

To a suspension of 0.443 g of the 7-amino-3-thiadiazole benzyhydryl ester obtained in Example 78 in 2 ml of anisole is added 3 ml of trifluoroacetate acid under stirring and ice-cooling. After 30 minutes, the solvent is distilled off under reduced pressure. The residue is dissolved in 10% hydrochloric acid and the solution is neutralized with a saturated aqueous solution of sodium bicarbonate. The formed precipitates are filtered, and washed with water, acetone and then ether to give 0.21 g of 7-amino-3-(5-methyl-1,3,4-thiadiazol-2-yl)-3-cephem-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04182866
Source datasetuspto-grants-1980_01
ORD IDord-a4ccf762d8e846a4b3a2b3074741a5cb
Source noteuspto-grants-1980_01