HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27222Generated: October 25, 2026
Isopropylamine → 1,3,5-Triazin-2-amine, 4,6-dichloro-N-(1-methylethyl)-
https://huagongshe.com/reaction/27222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,3,5-Triazin-2-amine, 4,6-dichloro-N-(1-methylethyl)- | HCID 19453 | — |
Reaction Steps
A suspension of 369 g of cyanuric chloride in 1000 ml of ethyl acetate is cooled to -15° C. With good stirring, 124 g of isopropylamine are first added dropwise at -20° C. to -10° C. in the course of 21/2 hours, followed by 267 g of a 30% aqueous solution of sodium hydroxide in the course of one hour. The reaction mixture is stirred for a further 11/2 hours at the same temperature, then the organic phase is separated, washed with two 100 ml portions of water and dried over sodium sulphate. The solvent is evaporated, to yield an oil from which the 2,4-dichloro-6-isopropylamino-s-triazine precipitates in crystalline form after stirring with petroleum ether at low temperature. Melting point: 46°-47° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04220770 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-32cef9d776e644fa9ed2f82788d54e0e |
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| Source note | uspto-grants-1980_09 |
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