HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550235Generated: October 26, 2026
Triethylsilane → 2-(4-Bromonaphthalen-2-ylmethyl)-5-fluorobenzo[b]thiophene
https://huagongshe.com/reaction/550235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (4-Bromo-naphthalen-2-yl)-(5-fluorobenzo[b]-thiophen-2-yl)methanol | HCID 67156712 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Bromonaphthalen-2-ylmethyl)-5-fluorobenzo[b]thiophene | HCID 67156577 | 215.5% |
Reaction Steps
In a nitrogen stream, triethylsilane (0.18 ml, 2.11 mmol) and a boron trifluoride-diethyl ether complex (0.25 ml, 1.94 mmol) were added to a solution of (4-bromo-naphthalen-2-yl)-(5-fluorobenzo[b]-thiophen-2-yl)methanol (260 mg, 0.65 mmol) in methylene chloride (10 ml) at 0° C. and the mixture was stirred a room temperature for two hours. A saturated sodium hydrogen carbonate aqueous solution was added and the mixture was extracted with methylene chloride. The organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous magnesium sulfate), and then the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:100)] to obtain the title compound (520 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943748B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-6e649d73c71c447597e84b19ea0769e8 |
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| Source note | uspto-grants-2011_05 |
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