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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440290Generated: October 30, 2026

Dichloromethane → N,N'-Dicyclohexylurea

https://huagongshe.com/reaction/440290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPentanoic AcidHCID 7991—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-(4-Nitrophenyl)-4-methyl-7,8-methylenedioxy-3,4-dihydro-5H-2,3-benzodiazepineHCID 10336422—
ProductN,N'-DicyclohexylureaHCID 4277—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of a 2.5 g (7.68 mmol) portion of the product of Example 26 in 40 ml of anhydrous dichloromethane 4.75 g (23 mmol) of dicyclohexylcarbodiimide and 2.88 g (23 mmol) of n-valeric acid were added and the reaction mixture was maintained at 25° C. under intermittent stirring for 24 hours. Then the N,N'-dicyclohexylurea formed as by-product was filtered, the filtrate was evaporated under reduced pressure, the residue was mixed with 2×40 ml of distilled water, decanted and the wet product was left to solidify under 50 ml of 50% ethanol. The solid compound was filtered, washed with 2×10 ml of 50% ethanol and dried at 80° C. The raw product obtained was recrystallized from 24 ml of ethanol and the crystals were dried at 100° C. to yield 2.20 g (70%) of the aimed product as a yellow powder, m.p.: 145°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519019
Source datasetuspto-grants-1996_05
ORD IDord-3ca221f9f8e346239f756bc9869b1755
Source noteuspto-grants-1996_05