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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112105Generated: November 4, 2026

Ethyl formate → HCID 178448642, compound

https://huagongshe.com/reaction/1112105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl formateHCID 8025—
Reactant3-Amino-1-butylthioureaHCID 1810303—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductHCID 178448642HCID 17844864255%

Reaction Steps

4-n-Butylthiosemicarbazide (20.0 g. or 0.136 mole) was heated to reflux with a solution of methanol (100 ml.), sodium methoxide (7.55 g. or 0.140 mole) and ethyl formate (20.7 g. or 0.280 mole). After 8 and 16 hours, 10 ml. and 5 ml. of ethyl formate was added to the refluxing solution. After 24 hours total reflux, the solvent was removed under reduced pressure and the residue was dissolved in water (100 ml.). The pH of the solution was adjusted to about 12 with 50% sodium hydroxide solution. This solution was then heated on a steam bath for 45 minutes, cooled and acidified with dilute hydrochloric acid. The resulting oil was extracted into ether. The ether was dried over sodium sulphate and removed under vacuum. The resulting oil was crystallized from ether-hexane to give 11.8 g. (55% yield) of 3-mercapto-4-n-butyl-1,2,4-triazole, m.p. 67°-69° C. The structure was confirmed by its nuclear magnetic resonance spectrum and its mass spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04120864
Source datasetuspto-grants-1978_10
ORD IDord-3cfe4e1e47bb41f3ac2bffb27db776f7
Source noteuspto-grants-1978_10