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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266201Generated: October 26, 2026

Phenol → 4-Bromo-2-(cyclopentyloxy)-1-methoxybenzene

https://huagongshe.com/reaction/266201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantDiethyl EtherHCID 3283—
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
SolventHexaneHCID 8058—
Product4-Bromo-2-(cyclopentyloxy)-1-methoxybenzeneHCID 997039298%

Reaction Steps

Cyclopentyl bromide (37 mL, 0.345 mol) was added to a slurry of the phenol (50 g, 0.246 mol) and potassium carbonate (17 g, 0.123 mol) in acetonitrile (500 mL) at reflux temperature. After two hours, cyclopentyl bromide (13.2 mL, 0.123 mol) and potassium carbonate (8.5 g, 0.062 mol) were added to complete the reaction (1 hour). Reaction progress was monitored by TLC (50% ethyl ether in hexane). The suspension was filtered. The filtered material was washed with ethyl acetate (2×100 mL). The filtrates were combined, concentrated and distilled under vacuum (0.1 mm, 140° C.°145° C.) to yield 65.62 g (0.242 mol, 98%) of product,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650444
Source datasetuspto-grants-1997_07
ORD IDord-8abaebbb46e1445bad126d16a9e0e76a
Source noteuspto-grants-1997_07