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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903900Generated: October 30, 2026

Allyl bromide → HCID 23331860, compound

https://huagongshe.com/reaction/903900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantSodiumHCID 5360545—
ReactantHCID 12766906HCID 12766906—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23331860HCID 2333186079%

Reaction Steps

34 g (0.1 mol) of 1-(4-bromophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol were suspended in 175 ml of dioxane and the suspension was added dropwise to a mixture of 3.5 g of 80% strength sodium hydride and 125 ml of dioxane while stirring. Thereafter, the mixture was heated under reflux for one hour. After cooling, 14.5 g (0.12 mol) of allyl bromide were added dropwise at room temperature to the sodium salt thus obtained. The mixture was then heated under reflux for 15 hours, allowed to cool and concentrated by distilling off the solvent. The oily residue was taken up in 600 ml of methylene chloride and the methylene chloride solution was washed twice with 1,000 ml of water each time, dried over sodium sulphate and concentrated. The residue was distilled under a high vacuum. 30 g (79% of theory) of 2-allyloxy-1-(4-bromophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butane of boiling point 152°-154° C./0.2 mm Hg were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229459
Source datasetuspto-grants-1980_10
ORD IDord-95d89c183bf44e2aba283834225d2e9f
Source noteuspto-grants-1980_10