戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 28449作成日:2026年10月24日

Diisopropylamine → 2,2,6-Trimethyl-heptanoic acid methyl ester

https://huagongshe.com/ja/reaction/28449

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物Methyl isobutyrateHCID 11039—
反応物2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
反応物1-Iodo-4-methylpentaneHCID 527581—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物2,2,6-Trimethyl-heptanoic acid methyl esterHCID 2167847999.4%

反応条件

温度-78 °C

反応手順

To diisopropyl amine (1.54 mL, 11.03 mmol) in THF (22 mL) at −78° C. was added nBuLi (6.89 mL of a 1.6 M solution in hexane). The solution was stirred for 30 min at −78° C., followed by the addition of methyl isobutyrate (0.97 mL, 8.48 mmol). The mixture was stirred at −78° C. for 2 h, and then 1-iodo-4-methyl pentane (1.8 g, 8.48 mmol) and DMPU (0.55 mL, 4.24 mmol) in THF (6 mL) was added. The reaction was stirred at −78° C. and allowed to slowly reach ambient temperature over 16 h. The reaction was quenched by the addition of ammonium chloride (saturated aqueous solution), and the mixture was extracted with EtOAc (2×10 mL). The organics were combined, washed with water, dried (MgSO4), filtered and concentrated. Silica gel chromatography (99/1 hexane/EtOAc) provided 1.57 g of 2,2,6-Trimethyl-heptanoic acid methyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419981B2
出典データセットuspto-grants-2008_09
ORD IDord-35517808fb2c4f85bbc4e95e78c9c6e4
出典メモuspto-grants-2008_09