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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1694768생성일: 2026년 10월 26일

Hydrochloric Acid → Methyl 6-bromo-5,5,6,6-tetrafluoro-2-(3,3,3-trifluoropropylsulfonyl)hexanoate

https://huagongshe.com/reaction/1694768

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물1,4-Dibromo-1,1,2,2-tetrafluorobutaneHCID 87719—
반응물Methyl 2-(3,3,3-trifluoropropylsulfonyl)acetateHCID 57425720—
용매Dimethyl SulfoxideHCID 679—
생성물Methyl 6-bromo-5,5,6,6-tetrafluoro-2-(3,3,3-trifluoropropylsulfonyl)hexanoateHCID 5937091027.2%

반응 단계

To a solution of 1.2 g of 1,4-dibromo-1,1,2,2-tetrafluorobutane and 1.0 g of methyl (3,3,3-trifluoropropylsulfonyl)acetate in 30 ml of dimethyl sulfoxide was added 0.2 g of sodium hydride (60% in oil) at room temperature. The mixture was stirred at the same temperature for 3 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 0.50 g of methyl 6-bromo-5,5,6,6-tetrafluoro-2-(3,3,3-trifluoropropylsulfonyl)hexanoate (hereinafter referred to as the present compound (4)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08158829B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-0940b8c9ec2a4bc481aa1c46454dd26c
출처 메모uspto-grants-2012_04