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HRID 520414作成日:2026年10月27日

Diisopropylamine → Tert-butyl((1,2-dimethoxyprop-1-en-1-yl)oxy)dimethylsilane

https://huagongshe.com/reaction/520414

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Propanoic acid, 2-methoxy-, methyl esterHCID 86599—
反応物Lithium diisopropylamideHCID 2724682—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl((1,2-dimethoxyprop-1-en-1-yl)oxy)dimethylsilaneHCID 86130319—

反応条件

温度-20 °C

反応手順

A solution of methyl 2-methoxypropionate (177 mg, 1.5 mmol) in THF (1 mL) was added to a solution of LDA prepared from diisopropylamine (0.212 mL, 1.50 mmol) and butyllithium (0.60 mL, 1.50 mmol) in THF (2 mL) at −78° C. under nitrogen. The mixture was gradually allowed to warm to −20° C. over 1 h, re-cooled to −78° C. and then a solution of tert-butylchlorodimethylsilane (233 mg, 1.50 mmol) in THF (1 mL) was added. The mixture was allowed to warm to rt over 2 h and stirred overnight. The reaction was quenched with satd. NaHCO3 (5 mL), diluted with DCM (10 mL). The organic layer was separated, washed with water, brine and dried (MgSO4). Evaporation of solvents afforded tert-butyl((1,2-dimethoxyprop-1-en-1-yl)oxy)dimethylsilane as a clear oil and used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09326973B2
出典データセットuspto-grants-2016_05
ORD IDord-842df4223b95441b84cabe8d66a92937
出典メモuspto-grants-2016_05