HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → 1-Bromo-4-phenylmethoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzyloxyphenylboric acid | HCID 15389139 | — |
| Reactant | 3-Bromo-4-cyclohexylmethyloxybenzaldehyde | HCID 22559082 | — |
| Product | 1-Bromo-4-phenylmethoxybenzene | HCID 138835 | — |
Reaction Steps
The intermediate 32 (1.76 g), 4-benzyloxyphenyl boric acid [6.75 g, 4-benzyloxy bromobenzene was prepared according to a process described in the process c-1 in example 1 from 4-bromophenol (Tokyo Chemical Ind. Co., Ltd.) and benzyl chloride (Tokyo Chemical Ind. Co., Ltd.), and the product was prepared according to a method described in the reference Y Satoh et al. SYNTHESIS page 1146, 1994], anhydrous potassium carbonate (4.09 g) and tetrakis (triphenylphosphine)palladium (0)(342 mg) were reacted according to the method described in the process i in example 23 to obtain the compound in the title (2.30 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376546B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-6b84389881e34620a6fc5bc7e27c64ee |
| Source note | uspto-grants-2002_04 |