HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309107Generated: November 4, 2026
Water → 4,6-Bis(difluoromethoxy)-2-(methylsulfanyl)pyrimidine
https://huagongshe.com/reaction/2309107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 178503558 | HCID 178503558 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 4,6-Bis(difluoromethoxy)-2-(methylsulfanyl)pyrimidine | HCID 11043427 | 86.7% |
Reaction Steps
14.0 g (0.067 mole) of 4-difluoromethoxy-6-hydroxy-2-methylthiopyrimidine are suspended in 18 ml of 50% potassium hydroxide solution, 10 ml of water and 160 ml of dioxane. After the addition of 0.5 g of 18-crown-6, the reaction mixture is heated to 40° C., and 20 g of chlorodifluoromethane are subsequently introduced over 5 hours. The aqueous phase is then separated and the organic phase is distilled under a high vacuum, affording 15.0 g (86.4% of theory) of 4,6-bis-difluoromethoxy-2-methylthiopyrimidine with a boiling point of 63° C./0.06 mbar. The substance melts at 46°-48° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04692524 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-06b35c91d2a340f78aee0780c3f9c475 |
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| Source note | uspto-grants-1987_09 |
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