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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

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-ButanesulfinamideHCID 3382465—
反応物1-(tert-Butyldimethylsilyloxy)-2-propanoneHCID 4124969—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium chloride; waterHCID 57417360—
生成物(NE)-N-[1-[tert-butyl(dimethyl)silyl]oxypropan-2-ylidene]-2-methylpropane-2-sulfinamideHCID 8738876765.2%

反応条件

温度70 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08349849B2
出典データセットuspto-grants-2013_01
ORD IDord-1505c45d2ade4cbf874a105cbbd7da47
出典メモuspto-grants-2013_01