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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399698Generated: October 30, 2026

Allyl bromide → 7-Allyloxy-1,2-benzisothiazole

https://huagongshe.com/reaction/2399698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium hydrideHCID 24758—
ReactantBenzo[d]isothiazol-7-olHCID 19384356—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product7-Allyloxy-1,2-benzisothiazoleHCID 19384354—

Reaction Steps

2.0 g of 7-hydroxy-1,2-benzisothiazole are dissolved in 20 ml of THF, and 460 mg of sodium hydride (60%) are added to the mixture at 0° C. When the evolution of gas has ended, 1 ml of allyl bromide is added dropwise, the reaction mixture is stirred for one day at room temperature. Again, 1 ml of allyl bromide and 40 mg of sodium hydride are added, and the mixture is stirred for 2 days under reflux. The reaction mixture is poured into water, rendered basic using 1 N potassium hydroxide solution and extracted using ethyl acetate. The organic phase is washed with saline, dried over sodium sulfate, filtered and concentrated. Silica gel chromatography with ethyl acetate/hexane (1:5) as mobile phase gives 2.0 g of 7-allyloxy-1,2-benzisothiazole; nD20 =1.6039 .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451595
Source datasetuspto-grants-1995_09
ORD IDord-ef48314bc9a549dfb2a0cd91337951a6
Source noteuspto-grants-1995_09