HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727167Generated: October 29, 2026
Chlorotrimethylsilane → 7-(bromomethyl)-2,2-dimethyl-3H-1-benzofuran
https://huagongshe.com/reaction/727167
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | (2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-yl)methanol | HCID 2795472 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-(bromomethyl)-2,2-dimethyl-3H-1-benzofuran | HCID 4271936 | — |
Reaction Steps
Under a nitrogen atmosphere, a mixture of 8.7 grams (0.1 mole) of lithium bromide in 100 mL of acetonitrile is stirred, and 13.5 grams (0.125 mole) of trimethylsilyl chloride is added. Upon completion of addition, a solution of 8.9 grams (0.05 mole) of 2,3-dihydro-2,2-dimethylbenzofuran-7-ylmethanol in 50 mL of acetonitrile is added. Upon completion of addition, the reaction mixture is warmed to reflux, where it is stirred for about 18 hours. After this time the reaction mixture is cooled to ambient temperature and then is taken up in 200 mL of diethyl ether. The mixture is then washed with 25 mL of water and then with 25 mL of an aqueous solution saturated with sodium chloride. The organic layer is then dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue, yielding 2,3-dihydro-2,2-dimethylbenzofuran-7-ylmethyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05712281 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-894e28eac1c54dccba787ba1056089ff |
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| Source note | uspto-grants-1998_01 |
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