戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 218246作成日:2026年10月26日

Ammonium Chloride → 3-Ethyl-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-di(tert-butyldimethylsilyloxy)benzene

https://huagongshe.com/reaction/218246

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromideHCID 370917—
反応物2,3-Di(tert-butyldimethylsilyloxy)-4-ethyl benzaldehydeHCID 85996524—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物3-Ethyl-6-[(Z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-di(tert-butyldimethylsilyloxy)benzeneHCID 6013069021.5%

反応条件

温度0 °C

反応手順

A suspension of 3,4,5-trimethoxybenzyltriphenylphosphonium bromide (3.9 g, 7.5 mmol) in tetrahydrofuran (40 mL) was cooled to 0° C. and butyllithium (4.7 mL of a 1.6 N solution in hexane, 7.5 mmol) was added dropwise. The brick red solution was stirred at 0° C. for 20 min, then a solution of 12 (2 g, ca 5 mmol) in tetrahydrofuran (15 mL) was added dropwise. The temperature was allowed to rise to room temperature over 4 hours, than the reaction was poured into ethyl acetate (ca 150 mL) and NH4Cl sat (ca 100 mL) the phases separated and the organic layer re-extracted with AcOEt. The combined organic extracts were washed with brine, dried over sodium sulphate and the solvent removed under reduced pressure to give a crude which was purified by column (cyclohexane:AcOEt 9:1) to give 0.6 g of 13:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198302B2
出典データセットuspto-grants-2012_06
ORD IDord-1ad46038f5d04092a37b9eae33895dff
出典メモuspto-grants-2012_06