HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043215Generated: November 1, 2026
Benzyl Bromide → 6-(Benzyloxy)-2,3-difluorobenzaldehyde
https://huagongshe.com/reaction/1043215
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Difluoro-6-hydroxybenzaldehyde | HCID 21221031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(Benzyloxy)-2,3-difluorobenzaldehyde | HCID 53440898 | — |
Reaction Steps
A mixture of 2,3-difluoro-6-hydroxybenzaldehyde (0.93 g), (bromomethyl)benzene (1.11 g) and potassium carbonate (1.22 g) in N,N-dimethylformamide (15 mL) was heated at 70° C. overnight. After cooling to room temperature, the reaction mixture was partitioned between water and ethyl acetate. The organic layer was separated, and the aqueous layer was extracted with additional ethyl acetate three times. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was purified by flash chromatography on silica gel to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557983B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-d589bd2625f5466b949e60fd00af5eff |
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| Source note | uspto-grants-2013_10 |
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