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HRID 218250作成日:2026年10月27日

Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromide → 3-Methyl-6-[(z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-di(tert-butyldimethylsilyloxy)benzene

https://huagongshe.com/reaction/218250

反応式

関与物質

役割名称HCID仕込み量
反応物Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromideHCID 370917—
反応物2,3-Bis-tert-butyldimethylsilyloxy-4-methylbenzaldehydeHCID 87768584—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
溶媒Sodium chloride; waterHCID 57417360—
生成物3-Methyl-6-[(z)-2-(3,4,5-trimethoxyphenyl)vinyl]-1,2-di(tert-butyldimethylsilyloxy)benzeneHCID 6013067548.7%

反応条件

温度0 °C

反応手順

A suspension of 3,4,5-trimethoxybenzyltriphenylphosphonium bromide (1.77 g, 3.4 mmol) in tetrahydrofuran (40 mL) was cooled to 0° C. and butyllithium (2.1 mL of a 1.6 N solution in hexane, 3.39 mmol) was added dropwise. The brick red solution was stirred at 0° C. for 20 min, then cooled to −78° C. and a solution of 16 (0.86 g, 2.26 mmol) in tetrahydrofuran (15 mL) was added dropwise. The temperature was allowed to rise to room temperature overnight, than the reaction was poured into brine (100 mL, containing 5 mL of 1 n HCl) and extracted twice with tert-butylmethyl ether (ca 100+50 mL). 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 17:

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-18e381c1bb114dd0aeaf98be7402d914
出典メモuspto-grants-2012_06