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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539348생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/539348

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, 9 H), 1.81 (m, 6 H), 2.12 (d, 2 H), 3.33 (m, 1 H), 3.42 (s, 3 H), 6.94 (d, 1 H), 7.59 (dd, 1 H), 8.53 (m, 1 H); MS (ES+) m/z 415 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865911B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-8c27dd4fceca4ead89fb8c6b2efb2e63
출처 메모uspto-grants-2014_10