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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183238Generated: October 25, 2026

Benzoyl chloride → 1-Benzoyl-1,3-dicyclohexyl-O-(N-2-butylideneamino)-isourea

https://huagongshe.com/reaction/1183238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant1,3-Dicyclohexyl-O-(N-2-butylideneamino)-isoureaHCID 86664633—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product1-Benzoyl-1,3-dicyclohexyl-O-(N-2-butylideneamino)-isoureaHCID 8666464072.4%

Reaction Steps

To a solution of 1,3-dicyclohexyl-O—(N-2-butylideneamino)-isourea (Cmpd. 2) (7.34 g, 25 mmol) and 4-dimethylaminopyridine (100 mg) in dichloromethane (25 ml) and triethylamine (3.9 ml, 27.5 mmol) is added benzoyl chloride (3.58 g, 25.5 mmol). The mixture is stirred 6 h at room temperature, diluted with hexane (200 ml), washed with water (4×20 ml), dried over MgSO4 and evaporated. The residue is chromatographed on silica gel (hexanes-ethyl acetate 4:1) and the pure fractions are recrystallized from hexane to afford 7.2 g of the title compound as white crystals, mp 74-78° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664288B2
Source datasetuspto-grants-2014_03
ORD IDord-21e258fb824b4ce59a7c7ef969cdaf7f
Source noteuspto-grants-2014_03