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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963597Generated: October 26, 2026

Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea

https://huagongshe.com/reaction/963597

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-nitro-benzene 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 dimethylfornamide (DMF) at room temperature overnight. A white precipitate of dicyclohexyl urea was formed. The precipitate was filtered and 300 ml diethyl ether is added to the mother liquor. After about 10 minutes to 4 hours a gummy solid precipitated 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 numberUS05763573
Source datasetuspto-grants-1998_06
ORD IDord-026efef93e574517ab845ce0c86a20b3
Source noteuspto-grants-1998_06