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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291809Generated: October 30, 2026

Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea

https://huagongshe.com/reaction/2291809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantSodium 4-hydroxy-3-nitrobenzenesulfonateHCID 12598197—
ReactantN-maleimido-6-aminocaproic acidHCID 19361018—
SolventDimethylformamideHCID 6228—
ProductN,N'-DicyclohexylureaHCID 4277—

Reaction Steps

One molar equivalent (2.24 g) of 4-hydroxy-3-nitrobenzene sulfonic acid sodium salt (HNSA) was mixed together with one molar equivalent (2.06 g) of dicyclohexylcarbodiimide and one molar equivalent (2.10 g) of N-maleimido-6-aminocaproic acid in 25 ml of dimethylformamide (DMF) at room temperature overnight. A white precipitate of dicyclohexyl urea was formed. The precipitate was filtered and 300 ml diethyl ether was added to the mother liquor. After about 10 minutes to 4 hours a gummy solid precipitate from the mother liquor was formed. This solid was found to contain 58% of active HNSA ester and 42% of free HNSA.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04798787
Source datasetuspto-grants-1989_01
ORD IDord-5431ec571d734ad082095f9101234830
Source noteuspto-grants-1989_01