HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213565Generated: October 27, 2026
Benzyl Bromide → 4-[(4-Methoxyphenyl)methoxy]-3-(phenylmethoxy)benzaldehyde
https://huagongshe.com/reaction/2213565
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-Hydroxy-4-[(4-methoxyphenyl)methoxy]benzaldehyde | HCID 11230648 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[(4-Methoxyphenyl)methoxy]-3-(phenylmethoxy)benzaldehyde | HCID 21957508 | 71.4% |
Reaction Steps
Benzyl bromide (13.56 mL, 0.11 mol, 1.1 eq) was added to a solution of 3-hydroxy-4-[(4-methoxyphenyl)methoxy]benzaldehyde (26.91 g, 0.10 mL, 1 eq) and cesium carbonate (20.37 g, 0.06 mol, 0.6 eq) in N,N-dimethylformamide (150 mL). The reaction mixture was stirred overnight and then concentrated in vacuo. The residual solution was diluted with ethyl acetate (200 mL) and washed with water (200 mL), saturated sodium chloride solution (3×200 mL), and 0.5M aqueous sodium hydroxide (3×200 mL), then dried over sodium sulfate and evaporated in vacuo. This gave a gummy solid which was recrystallized from ethyl acetate and petroleum ether to give the product as a pale brown powder (25.93 g, 71%). 1H NMR (CDCl3) δ 9.81 (s, 1H, O═C—H), 5.21 (s, 2H, CH2Ar), 5.20 (s, 2H, CH2Ar), 3.84 (s, 3H, OCH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105554B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-8d89b83898284051b61678a6629c7fb6 |
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| Source note | uspto-grants-2006_09 |
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