Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | O-methylhydroxylammonium chloride | HCID 11639 | — |
| Reactant | HCID 14280157 | HCID 14280157 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 19966724 | HCID 19966724 | 43.1% |
Reaction Steps
66.6 g of a 1.6 molar solution of n-butyllithium (0.156 mol) in n-hexane were added dropwise to a solution of 6.5 g of O-methylhydroxylammonium chloride (78 mmol) in 200 ml of tetrahydrofuran at -10° C. Stirring was carried out for 10 minutes at -10° C., and 20 g of 4-methoxy-2-methylsulfonyl-6-trifluoromethylpyrimidine (78 mmol) were added to the cloudy solution. Stirring was carried out for 1 hour at 25° C., the reaction batch was introduced into 200 ml of water, and the organic phase was separated off, washed with water and dried. Removal of the solvent gave an oily, slightly impure product, which could be crystallized in pentane at -78° C. 7.5 g of the product (43% of theory) were obtained as colorless crystals of melting point. 44°-46° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05612286 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-9ae80900bb0f408e837ff93d13457e49 |
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| Source note | uspto-grants-1997_03 |
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