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HRID 79498作成日:2026年10月24日

Diisopropylamine → 4-Tert-butyl 1-methyl 2-(4-chlorobenzyl)succinate

https://huagongshe.com/ja/reaction/79498

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-Butyl bromoacetateHCID 79177—
反応物Methyl 3-(4-chlorophenyl)propanoateHCID 8027172—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物4-Tert-butyl 1-methyl 2-(4-chlorobenzyl)succinateHCID 6873369681.4%

反応条件

温度0 °C

反応手順

BuLi (5.2 mL, 1.6M in hexanes) was added to a 0° C. solution of diisopropylamine (0.91 g, 9.0 mmol) in THF (40 mL). The reaction mixture was then stirred at 0° C. for 30 minutes, and then cooled to −78° C. A solution of methyl 3-(4-chlorophenyl)propanoate (1.5 g, 7.5 mmol) in THF (8 mL) was added slowly, and the reaction mixture was stirred at −78° C. for 40 minutes. A solution tert-butyl 2-bromoacetate (4.4 g, 22.7 mmol) in THF (5 mL) was then added. The reaction was then stirred for 30 minutes at −78° C. and then warmed to room temperature and stirred overnight. The reaction was then quenched with saturated NH4Cl and concentrated to remove THF. The reaction was then extracted with EtOAc, and the combined extracts were dried (Na2SO4), filtered, concentrated, and dried in vacuo to give 4-tert-butyl 1-methyl 2-(4-chlorobenzyl)succinate (1.91 g, 81%) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841304B2
出典データセットuspto-grants-2014_09
ORD IDord-6674fe9f14df488cbb58d62056c61ab6
出典メモuspto-grants-2014_09