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HRID 51306作成日:2026年10月26日

Chlorotrimethylsilane → Ethyl 3-cyclohexyl-3-methylbutanoate

https://huagongshe.com/reaction/51306

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物Ethyl 3,3-dimethylacrylateHCID 12516—
反応物Ammonium ChlorideHCID 25517—
反応物HCID 178478990HCID 178478990—
触媒Cuprous chlorideHCID 62652—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-cyclohexyl-3-methylbutanoateHCID 22289815—

反応手順

Trimethylsilyl chloride (1.3 ml, 10.2 mmol), copper (I) chloride (30 mg, 0.3 mmol) and cyclohexylmagnesium chloride (4.6 ml, 2N in diethyl ether, 9.2 mmol) were added slowly to an ice-cooled solution of ethyl 3,3-dimethylacrylate (1 g, 8.5 mmol) in tetrahydrofuran (10 ml). The solution was stirred for 10 minutes, then allowed to warm to room temperature and stirred for an hour. Saturated aqueous ammonium chloride solution (10 ml) was added and the mixture was partitioned between water (10 ml) and diethyl ether (20 ml). The layers were separated and the aqueous phase was extracted with diethyl ether (2×10 ml). The combined organic extracts were dried (MgSO4) and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel using ethyl acetate:pentane(5:95) as eluant to afford the title compound, 1.2 g. 1H-NMR (CDCl3, 400 MHz) δ: 0.75 (m, 8H), 1.05-1.28 (m, 7H), 1.62 (m, 1H), 1.78 (m, 4H), 2.20 (s, 2H), 4.10 (q, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713496B2
出典データセットuspto-grants-2004_03
ORD IDord-34c3090648704563a602edad49707405
出典メモuspto-grants-2004_03