HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368895Generated: October 25, 2026
Hydrochloric Acid → 6-Methoxybenzo[b]thiophene-2-ethanol
https://huagongshe.com/reaction/1368895
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | 6-Methoxy-1-benzothiophene | HCID 13634237 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Methoxybenzo[b]thiophene-2-ethanol | HCID 23500640 | — |
Reaction Steps
Butyl lithium (0.27 mol of a 2.5 M solution) was added dropwise to 6-methoxy-benzo[b]thiophene [prepared analogous to the procedure described in J. Med. Chem. 1989, 32(12), 2548-2554] (0.25 mol) in tetrahydrofuran (1000 ml), stirred at −30° C. The mixture was stirred for 10 minutes at −30° C. Ethylene oxide (0.38 mol in 100 ml tetrahydrofuran) was added dropwise at −30° C. The mixture was allowed to warm to room temperature and stirred for 3 hours. The mixture was acidified with dilute HCl solution. The solvent was evaporated. The residue was diluted with water and this mixture was extracted with CH2Cl2. The separated organic layer was dried, filtered and the solvent evaporated. The residue was stirred in hexane, filtered off and dried, yielding 41.3 g 6-methoxybenzo[b]thiophene-2-ethanol (interm. 5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576640B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-9f1a0a28d1f940edab65e224616938fd |
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| Source note | uspto-grants-2003_06 |
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