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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588929Generated: October 27, 2026

2,4,5-Trimethoxybenzaldehyde → N-cyclohexyl-N-cyclopentyl-4-[hydroxy(2,4,5-trimethoxyphenyl)methyl]benzamide

https://huagongshe.com/reaction/1588929

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,5-TrimethoxybenzaldehydeHCID 20525—
Reactant4-bromo-N-cyclohexyl-N-cyclopentylbenzamideHCID 19754888—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductN-cyclohexyl-N-cyclopentyl-4-[hydroxy(2,4,5-trimethoxyphenyl)methyl]benzamideHCID 19754870—

Reaction Steps

To a cold (-70° C.), stirred solution of 4-bromo-N-cyclohexyl-N-cyclopentylbenzamide (1.5 g, 4.3 mmol) in THF (20 ml) was added slowly a solution of tertbutyllithium (5 ml of 1.7 M solution in pentane) under an Argon atmosphere. The reaction was stirred at -70° to -75° for 20 min. and a solution of 2,4,5-trimethoxybenzaldehyde (843 mg, 4.3 mmol) in THF (10 ml) was added dropwise over 30 min. The reaction was stirred at -70° to -75° for 30 min. and at room temperature for 1 hr. The reaction was quenched by the addition of water and the aqueous layer extracted three times with ethyl acetate. The combined organic layers were washed with water and dried (Na2SO4). The drying agent was filtered and the filtrate concentrated in vacuo to give the crude product. Purification was effected by chromatography on silica gel using mixtures of ethyl acetate and hexane. The product was isolated as a glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05223539
Source datasetuspto-grants-1993_06
ORD IDord-5d0d7e9bff4f43be89c0f6c5c292cc33
Source noteuspto-grants-1993_06