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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839044Generated: November 2, 2026

Potassium Hydroxide → HCID 86735743, compound

https://huagongshe.com/reaction/839044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-Thiopheneacetic acidHCID 15970—
ReactantPotassium 2-thienylacetateHCID 23696799—
ReactantHCID 54361407HCID 54361407—
SolventMethanolHCID 887—
ProductPotassium 2-thienylacetateHCID 23696799—
ProductHCID 86735743HCID 8673574386%

Reaction Steps

A solution of potassium thiolacetate is prepared by adding 495 ml. of 2N-methanolic potassium hydroxide (0.99 mole) during a period of 15 min. to a solution of 74.3 ml. of thiolacetic acid (79.1 g., 1.04 mole) and 500 ml. of methanol while maintaining a temperature of 1°-5° C. The methanolic potassium thiolacetate solution thus prepared is added over 0.5 hr. to a mixture of N-[3-(chloroacetylamino)benzoyl]glycine methyl ester (267.5 g., 0.94 mole) in 2 l. of methanol while maintaining a temperature of 0°-5° C. After stirring for a period of 1 hr. without cooling, the reaction mixture is warmed at 40°-45° C. for 2 hrs., cooled, and filtered. The material collected is sequentially washed with 50% methanol, water, and 50% methanol, and then air dried to afford 262.4 g. (86% yield) of N-[3-(acetylthioacetylamino)benzoyl]glycine methyl ester, m.p. 86°-88° C. Crystallization from methanol provides analytically pure N-[3-(acetylthioacetylamino)benzoyl]glycine methyl ester, m.p. 90.0°-92.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04093739
Source datasetuspto-grants-1978_06
ORD IDord-5860766d1f3444e7ac10ec77c7d59a8e
Source noteuspto-grants-1978_06