HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-(2,4-Bis(benzyloxy)-5-chlorophenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(5-Chloro-2,4-dihydroxyphenyl)ethan-1-one | HCID 17245119 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(2,4-Bis(benzyloxy)-5-chlorophenyl)ethanone | HCID 17963691 | 90% |
Reaction Steps
Benzyl bromide (30 mL) was added to a mixture of 1-(5-chloro-2,4-dihydroxy-phenyl)-ethanone (20 g, 0.107 moles) and potassium carbonate (37 g, 2.5 equiv) in acetonitrile (350 mL). The mixture was heated at reflux for 6 hours then allowed to cool and stirred overnight. The mixture was filtered and the solids were washed with dichloromethane (3×100 mL). The combined organic extracts were evaporated in vacuo to leave a pale yellow solid which was triturated with a mixture of hexane (350 mL)/ethyl acetate (15 mL) and filtered to give an off-white solid, 1-(2,4-bis-benzyloxy-5-chloro-phenyl)-ethanone (35.4 g, 90%). 1H NMR (400 MHz) consistent with structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705027B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-6be1f194950146c390e50efc8e6cab57 |
| Source note | uspto-grants-2010_04 |