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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1770957생성일: 2026년 10월 26일

Water → N-(5-Bromo-4'-methoxy-3H-spiro[benzofuran-2,1'-cyclohexane]-3-ylidene)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/1770957

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Tert-ButanesulfinamideHCID 3382465—
반응물(5-Bromo-2-fluorophenyl)(1-hydroxy-4-methoxycyclohexyl)methanoneHCID 67979505—
촉매Titanium tetraethoxideHCID 76524—
용매Ethyl AcetateHCID 8857—
용매HCID 178479889HCID 178479889—
생성물N-(5-Bromo-4'-methoxy-3H-spiro[benzofuran-2,1'-cyclohexane]-3-ylidene)-2-methylpropane-2-sulfinamideHCID 6797952065%

반응 단계

To a mixture of 5-bromo-4′-methoxy-3H-spiro[benzofuran-2,1′-cyclohexan]-3-one (Intermediate 12, 2.8 g, 9.00 mmol) and 2-methylpropane-2-sulfinamide (2.024 g, 16.20 mmol) in methyl THF (15 mL) was added titanium ethoxide (3.71 mL, 18.00 mmol) and the reaction was heated to reflux. After 21 h the reaction was allowed to cool to r.t. whereafter it was diluted with EtOAc (150 mL). Water (12 mL) was added dropwise over 10 min under vigorous stirring and then the mixture was left standing without stirring for 1.5 h. The solids were filtered off and the organics were evaporated. The crude product was purified by flash chromatography using a gradient of 0%-50% EtOAc in heptane, yielding 2.41 g of the title compound (65% yield): 1H NMR (500 MHz, CDCl3) δ ppm 1.33 (s, 9H), 1.81 (m, 6H), 2.12 (d, 2H), 3.33 (m, 1H), 3.42 (s, 3H), 6.94 (d, 1H), 7.59 (dd, 1H), 8.53 (m, 1H); MS (ES+) m/z 415 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09248129B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-26e04c2f4e9c4bed96bb115e9ad4d569
출처 메모uspto-grants-2016_02