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HRID 132624作成日:2026年10月27日

tert-Butylsulfinamide, (S)-(-)- → (S)-2-Methyl-propane-2-sulfinic Acid ((3S)-1,3-dimethyl-pentylidene)-amide

https://huagongshe.com/reaction/132624

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butylsulfinamide, (S)-(-)-HCID 11355477—
反応物(S)-4-methyl-hexan-2-oneHCID 12208763—
触媒Titanium tetraethoxideHCID 76524—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium chloride; waterHCID 57417360—
生成物(S)-2-Methyl-propane-2-sulfinic Acid ((3S)-1,3-dimethyl-pentylidene)-amideHCID 8659795663.4%

反応手順

A mixture of (S)-4-methyl-hexan-2-one (1.6 g, 14 mmol), (S)-2-methyl-propane-2-sulfinic acid amide (1.7 g, 14 mmol) and titanium(IV) ethoxide (6.4 g, 28 mmol) in THF (30 mL) was refluxed for 10 hours. Then the reaction mixture was poured into brine (150 mL). The mixture was filtered. The filtrate was extracted by EtOAc (3×70 mL). The EtOAc phase was removed under reduce pressure and the residue was purified by a silica gel column (Hexane/EtOAc 3:1) to give the titled compound (1.93 g, 63% yield) as a colorless oil: 1H NMR (CDCl3) δ 2.24 (m, 2H), 2.27 (s, 3H), 1.85 (m, 1H), 1.22 (m, 2H), 1.20 (s, 9H), 0.85 (m, 6H); MS (APCI) (M+1)+ 218.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07388023B2
出典データセットuspto-grants-2008_06
ORD IDord-b893801a673040d08b755176e997b607
出典メモuspto-grants-2008_06