참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl Ethyl Ketone | HCID 6569 | — |
| 반응물 | 2,2,3,3,3-Pentafluoropropanol | HCID 9872 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2,3-Dimethyl-4-nitropyridine-N-oxide | HCID 148223 | — |
| 용매 | Hexamethylphosphoramide | HCID 12679 | — |
| 생성물 | 2,3-Dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine-1-oxide | HCID 13654794 | — |
반응 단계
A mixture of 2,3-dimethyl-4-nitropyridine-1-oxide (2.0 g), methyl ethyl ketone (30 ml), 2,2,3,3,3-pentafluoropropanol (3.05 ml), anhydrous potassium carbonate (3.29 g) and hexamethylphosphoric acid triamide (2.07 g) was heated at 70-80° C. with stirring for 4.5 days. Then, the insoluble matter was filtered off and the filtrate was concentrated. Water was added to the residue and the mixture was extracted with ethyl acetate. The extract layer was dried over magnesium sulfate, then the solvent was distilled off, and the residue was applied to a silica gel column (50 g). Elution with chloroform-methanol (10:1) and recrystallization from ethyl acetate-hexane gave 2.4 g of 2,3-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine-1-oxide as colorless needles. Melting point 148-149° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06749864B2 |
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| 출처 데이터셋 | uspto-grants-2004_06 |
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| ORD ID | ord-cfd0985523954329ba0a8a210d647fb4 |
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| 출처 메모 | uspto-grants-2004_06 |
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