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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255735Generated: October 31, 2026

Formic Acid → HCID 53939076, compound

https://huagongshe.com/reaction/255735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 54560759HCID 54560759—
SolventWaterHCID 962—
ProductHCID 53939076HCID 5393907661.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of acetic anhydride (15.9 g.) and formic acid (7.15 g.) was stirred at 50° C. for an hour. After cooling, ethyl 2-(2-aminothiazol-4-yl)-2-(2-bromoethoxyimino)acetate (syn isomer, 25 g.) was added to the solution and stirred at room temperature for an hour. The resultant solution was poured into water and extracted with ethyl acetate twice. The extracts were washed with a saturated aqueous solution of sodium chloride, a saturated aqueous solution of sodium bicarbonate (three times) and a saturated aqueous solution of sodium chloride in turn, and dried over magnesium sulfate. After concentrating the solution in vacuo, the oily residue was triturated with a mixture of diisopropyl ether and diethyl ether. The precipitates were collected by filtration to give ethyl 2-(2-formamidothiazol-4-yl)-2-(2-bromoethoxyimino)acetate (syn isomer, 16.75 g.), mp. 95° to 98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698337
Source datasetuspto-grants-1987_10
ORD IDord-65e1eca9c2b64bbaba8088992a376882
Source noteuspto-grants-1987_10