HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 6461349, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Hydroxybenzamide | HCID 342403 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 6461349 | HCID 6461349 | — |
Reaction Steps
To a solution of 13.7 g of 3-hydroxybenzamide and 25.6 of benzyl bromide in acetone (400 ml) were added 25.6 g of potassium carbonate at RT. The mixture was then refluxed for 6 h after which time the reaction was completed according to TLC analysis (CH2Cl2/MeOH: 20/1). The reaction mixture was cooled to RT and partitioned between EtOAc and water, the organic layer was separated, dried over sodium sulphate and concentrated in vacuo. The crystalline residue obtained was suspended in n-hexane (200 ml), the crystals were filtered off under suction and dried in a vacuum to give 3-benzyloxy-benzamide as a white crystalline solid, mp 136°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06242601B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-09aca3f6a7064aa6bc245c5d9ae0d166 |
| Source note | uspto-grants-2001_06 |