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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 916531생성일: 2026년 10월 25일

Triethylamine → HCID 58596253, 화합물

https://huagongshe.com/reaction/916531

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물BisulfiteHCID 104748—
반응물2,3,4-TrifluorophenolHCID 123174—
반응물N,N-Diethylethanamine trihydrofluorideHCID 175505—
반응물2-(6-{4-n-Propylcyclohexyl}spiro[3.3]hept-2-ylidene)[1,3]dithianeHCID 58596254—
용매DichloromethaneHCID 6344—
생성물HCID 58596253HCID 58596253—

반응 단계

10.0 g (29.7 mmol) of the dithioacetal 6 are dissolved in 100 ml of dichloro-methane, and 2.6 ml (30.0 mmol) of trifluoromethanesulfonic acid are added dropwise with ice/common salt cooling. After 5 minutes, the cooling is removed, and the batch is stirred at room temperature for 45 minutes. The batch is subsequently cooled to −70° C., a mixture of 7.5 ml (54.0 mmol) of triethylamine and 6.67 g (45.0 mmol) of trifluorophenol in 30 ml of dichloromethane is added, and the mixture is stirred at −70° C. for 1 hour. 24.2 ml (0.150 mol) of triethylamine tris(hydrofluoride) are then added, and, after 5 minutes, 42.9 g (0.150 mol) of DBH, suspended in 60 ml of dichloromethane, are added in portions over the course of about 30 minutes. After 90 minutes, the batch is allowed to thaw and is hydro-lysed using 1 M sodium hydroxide solution and aqueous hydrogen sulfite solution. The organic phase is separated off, washed with saturated sodium chloride solution and dried over sodium sulfate. The solvent is removed under reduced pressure, and the residue is filtered through silica gel with n-heptane, giving the spiro compound 7 as a colourless solid of melting point: 43° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07270856B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-25a79e9603f9477286e0a964f64d4e1e
출처 메모uspto-grants-2007_09