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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Tert-Butanesulfinamide | HCID 3382465 | — |
| 反応物 | (5-Bromo-2-fluorophenyl)(1-hydroxy-4-methoxycyclohexyl)methanone | HCID 67979505 | — |
| 触媒 | Titanium tetraethoxide | HCID 76524 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | HCID 178479889 | HCID 178479889 | — |
| 生成物 | N-(5-Bromo-4'-methoxy-3H-spiro[benzofuran-2,1'-cyclohexane]-3-ylidene)-2-methylpropane-2-sulfinamide | HCID 67979520 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08865911B2 |
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| 出典データセット | uspto-grants-2014_10 |
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| ORD ID | ord-8c27dd4fceca4ead89fb8c6b2efb2e63 |
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| 出典メモ | uspto-grants-2014_10 |
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