HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417055Generated: October 29, 2026
Boron tribromide → Cyclopentyl-(3,5-dihydroxy-phenyl)-methanone
https://huagongshe.com/reaction/417055
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Cyclopentyl(3,5-dimethoxyphenyl)methanone | HCID 11543194 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Acetone cardice | HCID 18522661 | — |
| Product | Cyclopentyl-(3,5-dihydroxy-phenyl)-methanone | HCID 59496852 | 97.1% |
Reaction Steps
To a solution of cyclopentyl-(3,5-dimethoxy-phenyl)-methanone (234 mg) in anhydrous dichloromethane (5 mL) cooled in dry ice/acetone bath was added dropwise a solution of boron tribromide (4 mL of 1 M solution in dichloromethane). After the addition was completed, the cooling bath was removed and the reaction mixture was stirred at room temperature overnight. Unreacted boron tribromide was quenched with methanol. Then the reaction mixture was diluted with ethyl acetate and washed with water and brine. The organic extract was dried over anhydrous sodium sulfate, concentrated and purified on a silica gel column using ethyl acetate and hexanes to yield 200 mg of the title compound (97% yield). Note: the title compound decomposes on air. HRMS calcd for C12H14O3 [M+H]+ 207.1016, observed 207.1016.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088936B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-ae42b4a10d98408eb7b1bf4e0e384bea |
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| Source note | uspto-grants-2012_01 |
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