HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → 4-(2-Bromoethyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(2-Bromoethyl)benzaldehyde | HCID 11085135 | 40.8% |
Reaction Steps
To a solution of (2-bromoethyl)benzene (100 mmol, 18.5 g) in methylene chloride (185 ml) at 0° C. was added dropwise titanium tetrachloride (200 mmol, 22 ml). The mixture was stirred for 10 minutes and alpha,alpha-dichloromethyl methyl ether (100 mmol, 9 ml) was added dropwise. The reaction mixture was stirred at room temperature for 1 hour and poured into saturated NaHCO3 (1 liter). Ethyl acetate (750 ml) was added and the solution was filtered through diatomaceous earth, the organic layer separated, dried (Na2SO4) and solvent removed in vacuo. The residue was triturated with hexane to afford 8.7 g of title product; m.p. 49°-52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05120754 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-2c700caf6ec74e62a32937116f8de256 |
| Source note | uspto-grants-1992_06 |