HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → 3,5-Dichloro-2-phenethoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Dichlorosalicylaldehyde | HCID 66660 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,5-Dichloro-2-phenethoxybenzaldehyde | HCID 18353665 | 70% |
Reaction Steps
To 3,5-dichlorosalicylaldehyde (229 mg, 1.2 mmol) in DMF (5 ml) was added K2CO3 (1.06 g, 7.7 mmol) followed by (2-bromoethyl)benzene (0.14 ml, 1.0 mmol). The mixture was stirred under argon for five days then diluted with H2O (30 ml), extracted with Et2O (3×50 ml), dried (MgSO4), filtered, and concentrated in vacuo to give the title compound as a white powder (207 mg, 0.7 mmol, 70%); δH (CDCl3) 3.17 (2H, t), 4.31 (2H, t), 7.19-7.36 (5H, m), 7.60 (1H, d), 7.67 (1H, d), 9.95 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06320051B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-146b3c04bb1d4e34b285963a497c4d91 |
| Source note | uspto-grants-2001_11 |