HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058365Generated: October 31, 2026
Benzo(B)Thiophene → 1-Benzothiophene-3-carbaldehyde
https://huagongshe.com/reaction/1058365
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzo(B)Thiophene | HCID 7221 | — |
| Reactant | Butyl Dichloromethyl Ether | HCID 4278354 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 1-Benzothiophene-3-carbaldehyde | HCID 227328 | 15.2% |
Reaction Steps
To a solution of benzothiophene (1.08 g, 8.0 mmol) in carbon disulfide (20 mL) at 0° C. was added titanium tetrachloride (3 mL, 27.3 mmol) followed by dichloromethyl n-butyl ether (1.24 g, 7.9 mmol) slowly dropwise. The reaction mixture was warmed to 25° C. and stirred for 1.5 h. The reaction was quenched with conc. hydrochloric acid solution (1 mL), diluted with chloroform (60 mL) and washed with water (50 mL), saturated sodium bicarbonate solution (2×30 mL) and brine (30 mL). The organic layer was dried (MgSO4), filtered, concentrated and flash chromatographed (silica gel, 2.5-5% diethyl ether in petroleum ether) to afford benzothiophene-3-carboxaldehyde (195 mg, 15% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515124B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-d72e388e4ff94d02ad7a6da3d3f88ea1 |
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| Source note | uspto-grants-2003_02 |
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