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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422956Generated: October 30, 2026

Toluene → 1-Bromo-4-(cyclohexylmethoxy)benzene

https://huagongshe.com/reaction/422956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-BromophenolHCID 7808—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 14946075HCID 14946075—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-4-(cyclohexylmethoxy)benzeneHCID 2303164954.6%

Reaction Steps

To a solution of 4-bromophenol (6.0 g, 34.7 mmol), cyclohexylmethylphenol (4.3 ml, 34.7 mmol) and triphenylphosphine (9.1 g, 34.7 mmol) in tetrahydrofuran (100 ml) was added slowly a 40% solution of diethyl azodicarboxylate in toluene (15.1 ml, 34.7 mmol) in portions at 0° C. with stirring, and then the resulting mixture was stirred at room temperature for 3 hours. After stirring, the reaction mixture was evaporated in vacuo, and hexane was added to the residue. After filtration, the filtrate was evaporated in vacuo once again, and the residue was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:20) as the eluent to afford 1-bromo-4-(cyclohexylmethoxy)benzene (5.1 g, yield: 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101650B2
Source datasetuspto-grants-2012_01
ORD IDord-606a11e7031d41abb5889afe0e0a3322
Source noteuspto-grants-2012_01