Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 21981631 | HCID 21981631 | — |
| Reactant | HCID 22012272 | HCID 22012272 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22012183 | HCID 22012183 | 32.7% |
Reaction Steps
4-(1,2-Benzisothiazol-3-yl)butyric acid (C. Branca et al, Phytochemistry 14, 1975, 2545) (17 g) was dissolved in dry toluene (500 ml) and cooled to -10° C. Di-tert-butyl aluminium hydride (120 ml of an 1 M solution in toluene) was added dropwise at -10° C. followed by stirring for 2 h at room temperature. Dilute sulfuric acid (2 M, 300 ml) was added, the phases separated, the aqeous phase extracted with ether, and the combined organic phases dried over magnesium sulfate. Removal of solvents in vacuo left a viscous oil which was purified by column chromatography (silica gel, eluent: ether). 4-(1,2-Benzisothiazol-3-yl)-1-butanol (5.2 g) was obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06031099 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-20e08e865e094b6ca8a8acd7a38b0e3a |
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| Source note | uspto-grants-2000_02 |
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