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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946468Generated: November 3, 2026

Toluene → 3-[(4-chlorophenyl)methyl]-2-(1-methylethyl)-5,6,7,8-tetrahydrocyclohepta[d]imidazol-4(3H)-one

https://huagongshe.com/reaction/1946468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
Reactant2-(1-methylethyl)-5,6,7,8-tetrahydrocyclohepta[d]imidazol-4(1H)-oneHCID 58460222—
CatalystTetrabutylammonium BromideHCID 74236—
SolventSodium HydroxideHCID 14798—
Product3-[(4-chlorophenyl)methyl]-2-(1-methylethyl)-5,6,7,8-tetrahydrocyclohepta[d]imidazol-4(3H)-oneHCID 5846022645.5%

Reaction Steps

Tetrabutylammonium bromide (1.7 g) was added to a stirred mixture of Intermediate 2 (2 g) and 4-chlorobenzyl bromide (2.4 g) in sodium hydroxide 20% aq. (14.2 mL) and Toluene (7 mL). The RM was stirred at room temp under nitrogen atm for 3 hours. An excess of sat NH4Cl aq. solution was added and the mixture was extracted with EtOAc (3×30 ml). The organics were combined, dried (hydrophobic frit) and concentrated under vacuum. The residue was purified on silica using a cyclohexane:ethyl acetate 0-100% gradient. The desired fractions were combined and concentrated under vacuum to give the title compound (1.5 g). LC/MS MH+ 317, Rt 1.91 min (5 minute run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399444B2
Source datasetuspto-grants-2013_03
ORD IDord-297eec495c88479f9059138b8cecef72
Source noteuspto-grants-2013_03