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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzo[d]isothiazol-7-ol | HCID 19384356 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Allyloxy-1,2-benzisothiazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05451595 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-ef48314bc9a549dfb2a0cd91337951a6 |
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| Source note | uspto-grants-1995_09 |
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