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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855760Generated: November 1, 2026

Acetic Acid → HCID 12837897, compound

https://huagongshe.com/reaction/1855760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant2-Thiopheneacetic acidHCID 15970—
ReactantHCID 12837905HCID 12837905—
ProductHCID 12837897HCID 12837897—

Reaction Steps

The triethylamine salt of thiolacetic acid was made by adding 2.23 g. (0.022 mole) of triethylamine to a stirred and ice-cooled solution of 1.67 g. (0.022 mole) of thiolacetic acid in 15 ml. of dimethylformamide. This solution was in turn added dropwise with stirring and ice-cooling to a solution of 4.2 g. (0.02 mole) of the compound prepared in Step B. above in 15 ml. of dimethylformamide, while maintaining the temperature below 10° C. The reaction mixture was stirred an additional hour, and then there was added 1 ml. of acetic acid. The reaction mixture was poured onto ice and a thick yellow oil formed. The mixture was decanted, and the ice was washed with water and again decanted. The yellow oil was taken up in 75 ml. of ether, dried, and evaporated, leaving 2.5 g. of yellow oil. This was chromatographed on a Waters high pressure liquid chromatography apparatus using 25% ethylacetate in hexane as the eluent. A water-white oil weighing 1.9 g. was obtained. A seed was formed by rubbing a little with petroleum ether and the bulk of material precipitated quickly to yield 1.6 g. of material having an m.p. of 96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04216160
Source datasetuspto-grants-1980_08
ORD IDord-f01ef50ac4c349b0a952c5ea43e1d3da
Source noteuspto-grants-1980_08