HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493459Generated: October 31, 2026
Dicyclohexylcarbodiimide → N,N'-Dicyclohexylurea
https://huagongshe.com/reaction/1493459
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Triethylenetetraminehexaacetic acid | HCID 70088 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N,N'-Dicyclohexylurea | HCID 4277 | — |
Reaction Steps
To a solution consisting of 0.7 g (1.3 mmol) N,N'-(2-aminoethyl) trans-1,2-diaminocyclohexane-N,N',N",N'",N'"hexaacetic acid in 50 ml dimethylsulfoxide was added 0.9 g (7.8 mmol) N-hydroxysuccinimide and 0.8 g (3.9 mmol) dicyclohexylcarbodiimide. This was stirred at room temperature for 48 hr., during which the white fluffy solid of dicyclohexyl urea formed. This solid was removed by filtration and the filtrate was concentrated to a thick oil under reduced pressure. A solid precipitated from the oil upon the addition of acetonitrile. This solid was collected, washed with cold acetonitrile and dried under vacuum to give 0.54 g of a light brown solid. NMR showed an average of 2 NHS esters so the yield is 56%. No further purification of the solid was attempted; mp 125°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05021571 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-2afdaad5e4ef4ac9be98e60a4c91f1a9 |
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| Source note | uspto-grants-1991_06 |
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