HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → Acetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2',4',6'-Trihydroxyacetophenone | HCID 68073 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Acetophenone | HCID 7410 | — |
Reaction Steps
To a solution of 1.68g of phloroacetophenone and 12.7 g of benzyl chloride in 20 ml of DMF is added 5.53 g of anhydrous K2CO3. The mixture is stirred for 16 hours at 65° under argon. The mixture is diluted with 100 ml of 5% NaCl and extracted with ethyl acetate (2 × 50 ml). The extracts are washed with 5% NaCl and 2% NaOH, dried over MgSO4 and concentrated to a red oil which is purified on a dry 250 g silica gel columning CCl4 as eluent. This yields 2,4,6-tribenzyloxyacetophenone as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04013801 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-37b556da94d4454a8425a0e130f35973 |
| Source note | uspto-grants-1977_03 |