HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807329Generated: November 4, 2026
Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea
https://huagongshe.com/reaction/1807329
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | 5-Fam | HCID 123755 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N'-Dicyclohexylurea | HCID 4277 | — |
Reaction Steps
A synthetic aldehyde, Pro4-de novo CHO, was prepared as follows. To a stirred solution of 5-carboxyfluorescein (5-FAM) (190 mg, 0.51 mmol) in anhydrous N,N-dimethylformamide (DMF (5 mL) were added N-hydroxysuccinimide (NHS) (77 mg, 0.67 mmol) and 1,3-dicyclohexylcarbodiimide (DCC) (126 mg, 0.61 mmol). After approximately 5 minutes, a white solid (dicyclohexylurea) started forming. The reaction mixture was stirred overnight under nitrogen. Thin layer chromatography (TLC) (40:9:1 CH2Cl2—CH3OH-water) indicated complete disappearance of the starting material. The mixture was then filtered, and the filtrate was added dropwise to a stirred solution of ethylene diamine (46 mg, 0.77 mmol) in DMF (3 mL). A solid was obtained. As evident from TLC, the reaction was complete instantaneously. This reaction mixture was subsequently treated with glyoxylic acid NHS ester prepared below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357277B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-a5d04c78dd564e37bf6947c1812cc9a7 |
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| Source note | uspto-grants-2013_01 |
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