HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837480Generated: October 25, 2026
3-Acetylbenzothiophene → 1-(1-Benzothiophen-3-yl)ethan-1-ol
https://huagongshe.com/reaction/1837480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Acetylbenzothiophene | HCID 14316 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(1-Benzothiophen-3-yl)ethan-1-ol | HCID 12992769 | 94% |
Reaction Steps
To a solution of 3-acetyl thianaphthene (2.024 g, 11.5 mmol) in ethanol (15 mL) was added sodium borohydride (0.434 g, 11.5 mmol). The mixture was stirred at 20° C. for 4 hours then evaporated, diluted with brine and extracted 3 times with ethyl acetate. The combined organics were dried over sodium sulfate, filtered and evaporated to give the intermediate title compound as a clear oil (1.924 g, 94%) which was used as is in subsequent reactions. FDMS m/e=178 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06784180B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-ac322796d8124832b218352dbbf93bff |
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| Source note | uspto-grants-2004_08 |
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