참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | 6-Nitro-2H-1,4-benzoxazin-3(4H)-one | HCID 2763683 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-nitro-3,4-dihydro-2H-1,4-benzoxazine | HCID 7062225 | — |
반응 단계
To a suspension of 6-nitro-4-H-benzo[1,4]oxazin-3-one (7.84 g, 40.38 mmol) in tetrahydrofuran (100 mL) was added a solution of 2.0M borane-methyl sulfide complex in tetrahydrofuran (91 mL, 181 mmol). The mixture was heated to reflux for 4.5 hours then allowed to stir overnight at room temperature. Methanol was added slowly to react with unreacted borane-methyl sulfide complex, which resulted a violent evolution of gas. When this subsided, excess methanol was added and the solution heated to reflux. After 2 hours the solution was cooled, the solvent evaporated under vacuum, and the residue triturated with ethyl acetate/hexane. An orange solid was filtered off which was rinsed with hexane, to yield 6-nitro-3,4-dihydro-2H-benzo[1,4]oxazine as a solid product. More of the solid was recovered as a second crop from the filtrate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06858621B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
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| ORD ID | ord-67d4f4c14c9d4d6ca9700aa849fccfb8 |
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| 출처 메모 | uspto-grants-2005_02 |
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