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HRID 277654作成日:2026年10月25日

2-Methyl-3-buten-2-ol → HCID 22625558、化合物

https://huagongshe.com/reaction/277654

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-3-buten-2-olHCID 8257—
反応物Tris(trimethylsilyl)silaneHCID 123134—
触媒1,1'-Azobis(cyclohexanecarbonitrile)HCID 74978—
生成物HCID 22625558HCID 2262555875%

反応条件

温度110 °C

反応手順

A dried reaction flask equipped for magnetic stirring and fitted with a reflux condenser was flushed with nitrogen and charged with toluene (500 mL). Oxygen was purged from the system by passing a stream of nitrogen through the solvent, 2-methyl-3-buten-2-ol (43.1 g, 500 mmol), tris(trimethylsilyl)silane (25.0 g, 100 mmol), and 1,1′-azobis(cyclohexanecarbonitrile) (1.22 g, 5 mmol) were added to the flask, and the reaction mixture was heated for 20 hours at 110° C. with stirring. The resulting solution was concentrated under reduced pressure, and distillation under vacuum (bp 90-104° C. at 0.10 mm) afforded the title compound (25.1 g, 74%) as a colorless solid. The distilled product was characterized by the following NMR data: 1H NMR (CDCl3) δ 0.14 (s, 27 H), 0.70-0.80 (m, 2 H), 1.17 (s, 6 H), 1.30 (br s, 1 H), 1.45-1.55 (m, 2 H); 13C NMR (CDCl3) δ 1.06 (9 C), 1.24 (1 C), 28.35 (2 C), 42.99 (1 C), 71.64 (1 C); 29Si NMR (CDCl3) δ −80.90 (1 Si), −12.83 (3 Si).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358675B1
出典データセットuspto-grants-2002_03
ORD IDord-8b9aca523c30479c88171315d03aa37d
出典メモuspto-grants-2002_03