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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905336Generated: November 2, 2026

Propargyl bromide → HCID 14278843, compound

https://huagongshe.com/reaction/1905336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 14278842HCID 14278842—
SolventAcetonitrileHCID 6342—
ProductHCID 14278843HCID 1427884396.4%

Reaction Steps

Reacted at 80° C. for 6 hours with stirring were 1.2 g of 5-t-butyl-3-(4-chloro-2-fluoro-5-hydroxyphenyl)-1,3,4-oxadiazol-2-one, 0.76 g of 3-bromopropyne, 40 ml of acetonitrile, and 0.3 g of potassium carbonate. After cooling, the reaction product was filtered and the filtrate was subjected to vacuum distillation to remove the solvent. To the residue was added 30 ml of methylene chloride, and the solution was washed with a 5% aqueous solution of sodium hydroxide and then with water. Upon removal of the solvent by distillation, 1.31 g of 5-t-butyl-3-(4-chloro-2-fluoro-5-propargyloxyphenyl)-1,3,4-oxadiazol-2-one was obtained. Upon recrystallization from n-hexane, a compound having a melting point of 72°-73° C. was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04842640
Source datasetuspto-grants-1989_06
ORD IDord-99b05d4dcfc44093989241f1e8a7a938
Source noteuspto-grants-1989_06