HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181082Generated: November 2, 2026
Benzyl Bromide → 5-(Benzyloxy)-2-bromobenzaldehyde
https://huagongshe.com/reaction/1181082
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Bromo-5-hydroxybenzaldehyde | HCID 387179 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(Benzyloxy)-2-bromobenzaldehyde | HCID 10870024 | — |
Reaction Steps
A solution of 2-bromo-5-hydroxy-benzaldehyde (5.99 g, 29.8 mmol, Preparation 13 Step A) in DMF (50 mL) was treated with benzyl bromide (7.65 g, 44.7 mmol) and Cs2CO3 (15.1 g, 44.7 mmol). The resulting mixture was heated at 80° C. for 60 min and was quenched with water (200 mL). The mixture was extracted with EtOAc (2×100 mL), dried (Na2SO4), and concentrated to a residue, which was purified on silica gel chromatography (hexanes/EtOAc 9/1) to afford 5-benzyloxy-2-bromo-benzaldehyde as white solid in quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07282501B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-dbb74fd82e4a456ca3ea87b9e56004b9 |
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| Source note | uspto-grants-2007_10 |
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