HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanuric chloride → HCID 21312532, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 19609580 | HCID 19609580 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21312532 | HCID 21312532 | 37.8% |
Reaction Steps
36.9 g of cyanuric chloride in 200 ml of boiling acetone were slowly poured into 400 ml of ice water, whilst stirring. The temperature was maintained between 0° and 5° C. by means of external cooling. 71.6 g of 4-amino-2-tert.-butyl-6-methylphenol in 100 ml of acetone and 42.4 g of sodium carbonate in 100 ml of water were simultaneously added at 10° C. The mixture was stirred at 10° C. for one hour and then at room temperature for 16 hours. The reaction mixture was then poured into ice water and the precipitate was filtered off and recrystallised from ethanol. In this way, it was possible to isolate 35.5 g of white 2,4-bis-(3-tert.-butyl-5-methyl-4-hydroxyanilino)-6-chloro-1,3,5-triazine which melts at 214° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04161592 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-eb5fd1faeeff412cbba0c9bc4572c4ff |
| Source note | uspto-grants-1979_07 |