HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cesium carbonate → 3-(Phenylmethoxy)-4-[(4-trifluoromethylphenyl)methoxy]benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-(Bromomethyl)-4-(trifluoromethyl)benzene | HCID 123062 | — |
| Reactant | 3-Benzyloxy-4-hydroxybenzaldehyde | HCID 11020635 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(Phenylmethoxy)-4-[(4-trifluoromethylphenyl)methoxy]benzaldehyde | HCID 21957495 | 100.2% |
Reaction Steps
4-Trifluoromethylbenzyl bromide (0.17 mL, 1.09 mmol, 1 eq) was added dropwise to a stirred solution of 3-benzyloxy-4-hydroxybenzaldehyde (250 mg, 1.09 mmol, 1 eq) and cesium carbonate (357 mg, 1.09 mmol, 1 eq) in N,N-dimethylformamide (10 mL). The reaction mixture was stirred overnight, then diluted with ethyl acetate (30 mL) and washed sequentially with water (4×30 mL), 0.5M aqueous sodium hydroxide (30 mL), 10% HCl and brine. The organic solution was dried over sodium sulfate and evaporated in vacuo to give the product as a white powder (422 mg, 99%). 1H NMR (CDCl3) δ 9.82 (s, 1H, O═C—H), 5.28 (2H, s, CH2Ar), 5.21 (s, 2H, CH2Ph).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105554B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-98c037bea44a46479f90b1ca54aea9f3 |
| Source note | uspto-grants-2006_09 |