HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354076Generated: October 29, 2026
Boron trifluoride etherate → 6-Methoxy-1-benzothiophene
https://huagongshe.com/reaction/354076
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | (2,2-Diethoxyethyl)(3-methoxyphenyl)sulfane | HCID 13642516 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Methoxy-1-benzothiophene | HCID 13634237 | 60.3% |
Reaction Steps
To a solution of boron trifluoride etherate (14.45 mL, 115 mmol) in 2000 mL of methylene chloride stirring in a cold water bath 20° C. was added dropwise 1-(2,2-Diethoxy-ethylsulfanyl)-3-methoxy-benzene (28.2 gm, 110 mmol) dissolved in 500 mL of methylene chloride. The addition was complete in 3 hrs. and then the reaction was warmed to room temperature for a further 1.5 hrs. The reaction mixture was then quenched with saturated sodium bicarbonate solution. The organic layer was separated and the aqueous layer was back extracted several times with methylene chloride. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude product was chromatographed on silica gel (using a gravity column) using hexanes as the eluant to yield 10.9 gm of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06756388B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-b270f99e13d44743839d10850f071d65 |
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| Source note | uspto-grants-2004_06 |
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