Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 21996912 | HCID 21996912 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15022719 | HCID 15022719 | — |
Reaction Steps
4.7 g (0.278 mol) of gaseous ammonia were passed into a mixture of 38.0 g (0.147 mol) of 2-fluoro(chloro)-4-trifluoromethoxy-6-trifluoromethylpyrimidine in 150 ml of diethyl ether while stirring at from -75° to -70° C. in the course of 1 hour. Stirring was continued for 2 hours in each case at -75° C. and, after heating, at 25° C. The precipitate which separated out was filtered off under suction, after which the organic phase was extracted with water, dried and partially evaporated down. Chromatography over silica gel using methyl tert-butyl ether gave 20.4 g (56.1% of theory) of the title compound of melting point 47°-49° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591694 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-ab0f62c64c5d45d3829a6ebbc33b9061 |
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| Source note | uspto-grants-1997_01 |
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