HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550241Generated: October 30, 2026
Methanol → 2-(4-Bromo-1-methoxynaphthalen-2-yl-methyl)benzo[b]thiophene
https://huagongshe.com/reaction/550241
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Benzo[b]thiophen-2-yl-(4-bromo-1-methoxynaphthalen-2-yl)methanol | HCID 67156311 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Bromo-1-methoxynaphthalen-2-yl-methyl)benzo[b]thiophene | HCID 66608193 | 80% |
Reaction Steps
In a nitrogen stream, triethylsilane (2.48 ml, 15.5 mmol) and a boron trifluoride-diethyl ether complex (1.08 ml, 8.54 mmol) were added dropwise to a solution of benzo[b]thiophen-2-yl-(4-bromo-1-methoxynaphthalen-2-yl)methanol (3.1 g, 7.76 mmol) in methylene chloride (60 ml) at 0° C. and the reaction mixture was stirred at room temperature for two hours, and then a 50% methanol aqueous solution (1 ml) was added and furthermore water (30 ml) was added thereto. The resulting mixture was extracted with methylene chloride, and 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 (1:50)] to obtain the title compound (2.38 g, 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-eb65cff3a7e047a2abf5ebc044186c82 |
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| Source note | uspto-grants-2011_05 |
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