HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822973Generated: October 31, 2026
Hydrochloric Acid → 4-Cyano-7-hydroxy benzo[b]thiophene
https://huagongshe.com/reaction/1822973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium ethanethiolate | HCID 4459711 | — |
| Reactant | 4-Cyano-7-methoxy benzo[b]thiophene | HCID 22171123 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Cyano-7-hydroxy benzo[b]thiophene | HCID 22171189 | 99.3% |
Reaction Steps
To a solution of 4-cyano-7-methoxy benzo[b]thiophene (450 mg, 2.38 mmol, 1 equiv.) in dry DMF (20 mL) was added sodium ethanethiolate (80% technical grade, 1.34 g, ˜13 mmol, ˜5 equiv.) and the reaction mixture was heated at 150° C. for 2 hr. The mixture was cooled to room temperature and ethyl acetate and 1N HCl were added and the layers were separated. The aqueous layer was extracted with ethyl acetate and the combined organic extracts were washed with brine (3 times), dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The acquired material thus obtained was purified via medium pressure liquid chromatography eluting with 30% ethyl acetate/70% hexanes to afford the title compound (414 mg, 99%) as a colorless solid; □H (400 MHz, CD3OD) 6.80 (1H, d, J=8 Hz), 7.47 (1H, d, J=6 Hz), 7.64 (1H, d, J=8 Hz), 7.83 (1H, d, J=6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07037932B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-e55a3dc0c97448aab0497a7a63ac9f13 |
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| Source note | uspto-grants-2006_05 |
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