HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293437Generated: October 30, 2026
Benzyl Bromide → 4-Benzyloxy dibenzo[b,d]furan-1-carbaldehyde
https://huagongshe.com/reaction/1293437
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxy dibenzo[b,d]furan-1-carbaldehyde | HCID 44225196 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Benzyloxy dibenzo[b,d]furan-1-carbaldehyde | HCID 85967058 | 90.8% |
Reaction Steps
Intermediate 19 (1 gm, 5.10 mmol) was dissolved in dry DMF (10 ml). Anhydrous potassium carbonate (1.05 gm, 7.65 mmol) was added to the above solution and was stirred for 10 min. at 80° C. To this was added benzyl bromide (0.87 gm, 5.10 mmol) and the reaction mixture was stirred for 2 h. The reaction mixture was cooled to room temperature and diluted with water (100 ml) and extracted with ethyl acetate (3×50 ml). The organic extract was washed with water (50 ml) and brine solution (25 ml) and dried over anhydrous sodium sulfate. Removal of solvent gave the product as a brown solid (1.4 gm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238725B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-3d637748b5774261b7e6761ed5ec0bd7 |
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| Source note | uspto-grants-2007_07 |
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