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HRID 1802121作成日:2026年10月25日
Tert-Butanesulfinamide → (NE)-N-[1-[tert-butyl(dimethyl)silyl]oxypropan-2-ylidene]-2-methylpropane-2-sulfinamide
https://huagongshe.com/reaction/1802121
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Tert-Butanesulfinamide | HCID 3382465 | — |
| 反応物 | 1-(tert-Butyldimethylsilyloxy)-2-propanone | HCID 4124969 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Sodium chloride; water | HCID 57417360 | — |
| 生成物 | (NE)-N-[1-[tert-butyl(dimethyl)silyl]oxypropan-2-ylidene]-2-methylpropane-2-sulfinamide | HCID 87388767 | 65.2% |
反応手順
1-(tert-butyldimethylsilyloxy)propan-2-one (188 mg, 1.0 mmol) and Ti(OEt)4 (0.52 mL, 2.5 mmol) were dissolved in THF (5 mL). Then 2-methylpropane -2-sulfinamide (121 mg, 1.0 mmol) was added to the mixture under nitrogen atmosphere. The mixture was heated to 70° C. for 2 h. The mixture was poured into brine and filtered through a plug of Celite. The organic layer was concentrated and purified by silica gel chromatography using PE/EA (5/1) to give product the title compound (190 mg, 65%). EDI-MS (M+1): 292. 1H NMR (300 MHz, CDCl3) δ 4.152 (s, 2H), 2.248 (s, 3H), 1.156 (s, 9H), 0.839 (s, 9H), 0.001 (s, 6H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08349849B2 |
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| 出典データセット | uspto-grants-2013_01 |
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| ORD ID | ord-1505c45d2ade4cbf874a105cbbd7da47 |
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| 出典メモ | uspto-grants-2013_01 |
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