HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553214Generated: October 26, 2026
Sulfuric Acid → 2-(1-Benzothiophen-5-yl)ethan-1-ol
https://huagongshe.com/reaction/553214
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Benzo[b]thiophene-5-acetic acid | HCID 11469582 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(1-Benzothiophen-5-yl)ethan-1-ol | HCID 11983371 | 85.6% |
Reaction Steps
To 340 mL of tetrahydrofuran was suspended 50.2 g of sodium borohydride, to which were dropped tetrahydrofuran (340 mL) solution of 170 g of (1-benzothiophen-5-yl)acetic acid, and 65.1 g of sulfuric acid successively, which was then stirred at room temperature for 2.5 hours. To this reaction mixture was dropwise added 85 mL of acetone, which was then stirred for 30 minutes. Thereto were added 510 mL of water and 680 mL of toluene. The organic layer was separated, to which was added 510 mL of water, and the pH was adjusted to 12 with 48 mL of 20% (w/w) sodium hydroxide aqueous solution. The organic layer was separated, and washed with water, followed by distilling off the solvent. Thereto were added cyclohexane and toluene. The precipitate was collected by filtration to provide 135 g of 2-(1-benzothiophen-5-yl)ethanol as white solid form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951963B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-e293466984bb4d4184938ef19f57e46b |
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| Source note | uspto-grants-2011_05 |
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