戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 335216作成日:2026年10月26日

Diisopropylamine → Methyl 4-bromo-2-methoxy-2-methylpent-4-enoate

https://huagongshe.com/reaction/335216

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物2,3-DibromopropeneHCID 10552—
反応物Propanoic acid, 2-methoxy-, methyl esterHCID 86599—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-bromo-2-methoxy-2-methylpent-4-enoateHCID 86631519109.3%

反応条件

温度-78 °C

反応手順

A 500 mL round-bottom flask was charged with diisopropylamine (12.89 mL, 92.00 mmol) and dry THF (100 mL) and cooled to −78° C. Butyllithium (2.5 M in hexanes) (36.80 mL, 92.00 mmol) was added dropwise over 20 minutes and the mixture was agitated for additional 30 minutes. Methyl 2-methoxypropanoate (10.35 g, 87.61 mmol) was added dropwise over 20 minutes and the mixture was agitated for 30 minutes. 2,3-Dibromopropene (10.70 mL, 87.61 mmol) was added dropwise over 20 minutes, the mixture was agitated for 30 minutes and then allowed to warm up to ambient temperature and agitated for additional 2 hours. The reaction was quenched with saturated ammonium chloride solution and extracted twice with ether. Extracts were washed with sodium bicarbonate solution, brine, dried and evaporated to give the title compound (22.7 g, 98.4% yield) as pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883828B2
出典データセットuspto-grants-2014_11
ORD IDord-12a6afb9c809476f8edb0aaaa2d93ddc
出典メモuspto-grants-2014_11