HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194627Generated: November 2, 2026
Chlorodifluoromethane → HCID 14014318, compound
https://huagongshe.com/reaction/1194627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Diglyme | HCID 8150 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178463635 | HCID 178463635 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14014318 | HCID 14014318 | — |
Reaction Steps
A mixture of 200 g (1.02 moles) of 2-ethylamino-4-hydroxy-6-isopropylamino-1,3,5-triazine, 454 g (8.11 moles) of potassium hydroxide, 1150 ml of diethylene glycol dimethyl ether and 1150 ml of water was vigorously stirred, and heated to 90° C. Chlorodifluoromethane gas was blown into the reaction mixture until 2-ethylamino-4-hydroxy-6-isopropylamino-1,3,5-triazine was no longer detected by thin-layer chromatography. After the reaction, the reaction mixture was cooled to room temperature, extracted with methylene chloride. The methylene chloride layer was washed with water twice or thrice, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure. The crude product was chromatographed on a silica gel column. The column was eluted with n-hexane/ethyl acetate (5:1) to give 58.9 g of 2-difluoromethoxy-4-ethylamino-6-isopropylamino-1,3,5-triazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04816064 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-ff80153b410847d4914705e403cbc2e8 |
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| Source note | uspto-grants-1989_03 |
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