HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanuric chloride → HCID 178429403, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178429404 | HCID 178429404 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178429403 | HCID 178429403 | 97.2% |
Reaction Steps
An aqueous solution (40 ml) containing 6 ml of diisopropylethylamine and 5 g (0.018 mol) of 1-(4-aminobutyl)-3-(6-methyl-4-oxo-1,4-dihydropyrimidin-2-yl)urea, prepared beforehand, was added, dropwise, to 5 g (0.018 mol) of cyanuryl chloride suspended in 80 ml of acetonitrile, at a temperature of −20° C. The reaction medium was stirred for 12 hours at ambient temperature and then poured into 200 ml of ice-cold water. The precipitate formed was filtered off and then dried under vacuum, so as to give 6.8 g (0.0175 mol) of a yellow powder with a yield of 97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575341B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-9a07311878234075b68219d1396bf6fb |
| Source note | uspto-grants-2013_11 |