HuagongsheHuagongshe Chemistry Print Report · For research reference only
Difluoromethane → 2-Amino-4-chloro-6-difluoromethoxy-pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Difluoromethane | HCID 6345 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Amino-4,6-dichloropyrimidine | HCID 65522 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Amino-4-chloro-6-difluoromethoxy-pyrimidine | HCID 20185689 | — |
Reaction Steps
A suspension of 16.4 g of 2-amino-4,6-dichloropyrimidine in 100 ml of 40% sodium hydroxide solution is stirred for 1 hour at a temperature of 95° to 100° C. After the addition of 200 ml of dioxane, there are added at a temperature of 70° to 75° C., within 1 hour, 20 g of gaseous difluoromethane. The organic phase is separated, and concentrated to about 1/5 of its volume; it is then poured into water and the solid precipitate is removed. The yield is 6 g of 2-amino-4-chloro-6-difluoromethoxy-pyrimidine, m.p. 118° to 119° C. (compound No. 1.7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04480101 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-f9b034d86e7a4f48988df82a1abb1b11 |
| Source note | uspto-grants-1984_10 |