Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 888336생성일: 2026년 10월 26일
Hydrochloric Acid → 6,6,6-Trifluoro-2-methyl-2-(3,3,3-trifluoropropylsulfonyl)-4-hexenenitrile
https://huagongshe.com/reaction/888336
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4,4,4-Trifluoro-2-butenyl p-toluenesulfonate | HCID 53655839 | — |
| 반응물 | 2-(3,3,3-Trifluoropropylsulfonyl)propionitrile | HCID 57788363 | — |
| 생성물 | 6,6,6-Trifluoro-2-methyl-2-(3,3,3-trifluoropropylsulfonyl)-4-hexenenitrile | HCID 72281791 | — |
반응 단계
To a solution of 1.5 g of 4,4,4-trifluoro-2-butenyl p-toluenesulfonate and 1.2 g of 2-(3,3,3-trifluoropropylsulfonyl)propionitrile in 30 ml of tetrahydrofuran was added 0.2 g of sodium hydride (60% in oil) at room temperature. The reaction mixture was stirred at the same temperature for 2 days. To the reaction mixture was added 10% hydrochloric acid and then extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography to obtain 0.80 g of 6,6,6-trifluoro-2-methyl-2-(3,3,3-trifluoropropylsulfonyl)-4-hexenenitrile (hereinafter referred to as the present compound (34)).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08247595B2 |
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| 출처 데이터셋 | uspto-grants-2012_08 |
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| ORD ID | ord-4fb3e7227b194dea95a8f344ba55403c |
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| 출처 메모 | uspto-grants-2012_08 |
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