Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843033Generated: October 30, 2026

Benzyl Chloride → 1-Bromo-4-phenylmethoxybenzene

https://huagongshe.com/reaction/843033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
Reactant4-BromophenolHCID 7808—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Benzyloxyphenylboric acidHCID 15389139—
Reactant3-Bromo-4-cyclohexylmethyloxybenzaldehydeHCID 22559082—
Product1-Bromo-4-phenylmethoxybenzeneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376546B1
Source datasetuspto-grants-2002_04
ORD IDord-6b84389881e34620a6fc5bc7e27c64ee
Source noteuspto-grants-2002_04