HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272519Generated: November 2, 2026
Boron tribromide → 4-Cyclopropyl-3-fluoro-2-hydroxybenzaldehyde
https://huagongshe.com/reaction/2272519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Cyclopropyl-3-fluoro-2-methoxybenzaldehyde | HCID 90423252 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Cyclopropyl-3-fluoro-2-hydroxybenzaldehyde | HCID 90423572 | 90.3% |
Reaction Steps
Boron tribromide (1 M dichloromethane solution, 18.5 mL) was added at −78 C to a dichloromethane (70 mL) solution of 4-cyclopropyl-3-fluoro-2-methoxybenzaldehyde (1.79 g), and the mixture was stirred at the same temperature as above for 2 hours in a nitrogen atmosphere and then stirred at 0 C for 1 hour. A saturated aqueous solution of sodium bicarbonate was added to the reaction mixture at 0 C, and dichloromethane was distilled off under reduced pressure. The obtained residue was subjected to extraction with ethyl acetate. The obtained organic layer was washed with water and saturated saline in this order and dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (1.50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120777B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-1d4006afa2de4a21a1aa68dc376f7644 |
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| Source note | uspto-grants-2015_09 |
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