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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065793Generated: October 30, 2026

Allyl bromide → HCID 178460728, compound

https://huagongshe.com/reaction/1065793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178441225HCID 178441225—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 178460728HCID 17846072888%

Reaction Steps

To a slurry of 3-t-butylpyrazole-5-thiol (10 g) in dry dimethoxyethane (100 ml) was added portionwise, with stirring, sodium hydride (1.6 g). Stirring at room temperature was continued for a few minutes, and then allyl bromide (7.8 g) was added. The reaction mixture was stirred for 2 hours, filtered, and evaporated. The residue was dissolved in ether and washed with water, and the ether layer separated, dried, and evaporated to give 3-t-butyl-5-(allylthio)pyrazole, as a pale brown oil (11.0 g), 88% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04331678
Source datasetuspto-grants-1982_05
ORD IDord-625453a54a47419cb84bf051042b3648
Source noteuspto-grants-1982_05