HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372808Generated: October 26, 2026
Tin tetrachloride → (2-Butyl-3-benzo[b]furanyl) (5-methoxy-2-thienyl)methanone
https://huagongshe.com/reaction/2372808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 2-Butylbenzofuran | HCID 77951 | — |
| Reactant | 5-Methoxy-2-thiophenecarbonyl chloride | HCID 14721834 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | (2-Butyl-3-benzo[b]furanyl) (5-methoxy-2-thienyl)methanone | HCID 14721835 | — |
Reaction Steps
3.0 g (17.2 mmol) 2-butylbenzo[b]furan were dissolved in 30 ml abs. chloroform, the solution was cooled to 0° C., and reacted with 3.6 g (20.4 mmol) 5-methoxy-2-thiophenecarbonyl chloride, dissolved in 5 ml abs. chloroform, and then, at a temperature between 0° and 3° C., 2.8 ml SnCl4 were added dropwise. Stirring for 2 hours at 0° C. followed. The reaction mixture was evacuated under ice-cooling over 50 ml 2N HCl, the phases were separated and the aqueous phase thoroughly extracted with ether. The chloroform and ether phases were each washed with 50 ml 2N NaOH, combined, dried over sodium sulphate and evaporated. The crude product was quickly distilled.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05100911 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-3a67cd2fe798453f90f8e3841c0c8efd |
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| Source note | uspto-grants-1992_03 |
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