HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390970Generated: October 29, 2026
Hydrochloric Acid → 2-(1-Benzothiophen-5-yl)ethan-1-ol
https://huagongshe.com/reaction/2390970
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Benzo[b]thiophene-5-acetic acid | HCID 11469582 | — |
| Reactant | Hydrochloride 1,2-dimethoxyethane | HCID 86628724 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(1-Benzothiophen-5-yl)ethan-1-ol | HCID 11983371 | 84.6% |
Reaction Steps
To 5 mL of 1,2-dimethoxyethane was suspended 2.95 g of sodium borohydride, to which were dropwise added 1,2-dimethoxyethane (25 mL) solution of 10 g of (1-benzothiophen-5-yl)acetic acid, and 11 mL of 6.9 mol/L hydrochloride/1,2-dimethoxyethane solution, which was then stirred at room temperature for 1 hour. To this reaction mixture was dropwise added 5 mL of acetone, which was then stirred for 30 minutes. Thereto were added 20 mL of water, 30 mL of toluene and 2 mL of 2 mol/L hydrochloric acid. Next, after the pH was adjusted to 9.5 with 20 mL of 2 mol/L sodium hydroxide aqueous solution, the organic layer was separated. The organic layer was dried over anhydrous magnesium sulfate, followed by distilling off the solvent. Thereto were added cyclohexane and toluene. The precipitate was collected by filtration to provide 7.84 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 | US08273902B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-86f68d1aa9ad4e04b4be03c0f716db64 |
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| Source note | uspto-grants-2012_09 |
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