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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723342Generated: October 30, 2026

Propargyl bromide → HCID 20025630, compound

https://huagongshe.com/reaction/1723342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178527954HCID 178527954—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20025630HCID 20025630—

Reaction Steps

6 g of 2-mercapto-5-thienyl-1,3,4-thiadiazole are placed in 40 ml of dioxan and stirred for 15 minutes with 3.36 g of potassium tert.-butoxide. Subsequently, 5.9 g of propargyl bromide are added dropwise at 30° C. and the reaction mixture is stirred overnight at room temperature. The salts are filtered off, the filtrate is concentrated by evaporation, the residue is taken up in methylene chloride and the solution is washed with water and then with 1N sodium hydroxide solution. The solvent is removed in vacuo and the residue obtained is 6.1 g of crude title compound which, recrystallised from tert.-butyl methyl ether, yields the title compound having a melting point of 71°-73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04861787
Source datasetuspto-grants-1989_08
ORD IDord-ca9716c84af14dc4916e7c0987df6102
Source noteuspto-grants-1989_08