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HRID 539348作成日:2026年10月26日

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

https://huagongshe.com/reaction/539348

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Tert-ButanesulfinamideHCID 3382465—
反応物(5-Bromo-2-fluorophenyl)(1-hydroxy-4-methoxycyclohexyl)methanoneHCID 67979505—
触媒Titanium tetraethoxideHCID 76524—
溶媒Ethyl AcetateHCID 8857—
溶媒HCID 178479889HCID 178479889—
生成物N-(5-Bromo-4'-methoxy-3H-spiro[benzofuran-2,1'-cyclohexane]-3-ylidene)-2-methylpropane-2-sulfinamideHCID 6797952065%

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08865911B2
出典データセットuspto-grants-2014_10
ORD IDord-8c27dd4fceca4ead89fb8c6b2efb2e63
出典メモuspto-grants-2014_10