HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846851Generated: November 1, 2026
Cyanuric chloride → HCID 57314960, compound
https://huagongshe.com/reaction/846851
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | HCID 14533831 | HCID 14533831 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57314960 | HCID 57314960 | — |
Reaction Steps
To 50 g water in a 3-neck flask equipped with stirrer and a thermometer, were added 9.2 g (0.05m) of cyanuric chloride, dissolved in 50 g acetone below 10° C. To the white slurry of cyanuric chloride, 27.9 g of bis(2-hydroxyethyl) (iminodiethylene)biscarbamate (HEC), NH(CH2CH2NHCO2CH2CH )2 dissolved in 50 g of water was added over a period of 15 minutes. During the addition, the reaction temperature was maintained below 12° C. After complete addition of HEC, the slurry turned into a clear solution. To this was added 10% caustic to maintain the reaction pH at about 7 and the reaction mixture was allowed to warm up to 25° C. At 25° C., as the reaction progressed, a white crystalline solid slowly separated out. After 4 hrs. at 25-35° C, the solids were separated by filtration, washed with water and recrystallized from ethanol. The product yield was 24 g and m.p. 174° C. The structure of the product was confirmed by nuclear magnetic resonance (nmr) and fast atomic bombardment (fab), mass spectrometry to be that of FORMULA I: ##STR19##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05138055 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-b8c87196c1674229bade179f7be4d4d9 |
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| Source note | uspto-grants-1992_08 |
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