HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502502Generated: November 2, 2026
Ethanol → 2-(Benzo[b]thiophen-3-yl)ethanol
https://huagongshe.com/reaction/502502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Benzo[b]thiophene-3-acetic acid | HCID 70799 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Benzo[b]thiophen-3-yl)ethanol | HCID 15852206 | — |
Reaction Steps
A solution of benzo[b]thiophen-3-yl-acetic acid (6.0 g, 31.2 mmol) in 40 ml of tetrahydrofuran was added dropwise at RT to a suspension of lithium alanate (1.54 g, 41 mmol) in 35 ml of tetrahydrofuran. The mixture was stirred for 60 minutes at 60° C., and then excess alanate was hydrolysed with ethanol. The mixture was suction-filtered over Kieselguhr and the solvent was removed in vacuo. The product was obtained in the form of a yellowish oil in a yield of 5.1 g (92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776848B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-7d496dbea50649b3ba257d028bad7c01 |
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| Source note | uspto-grants-2010_08 |
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