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HRID 12485作成日:2026年10月25日

Ethyl 2-(2-methyl-1,3-dioxolan-2-yl)butanoate → 2-(2-Methyl-[1,3]dioxolan-2-yl)-butan-1-ol

https://huagongshe.com/reaction/12485

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-(2-methyl-1,3-dioxolan-2-yl)butanoateHCID 12948748—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒Diethyl EtherHCID 3283—
生成物2-(2-Methyl-[1,3]dioxolan-2-yl)-butan-1-olHCID 59735081—

反応手順

2-(2-Methyl-[1,3]dioxolan-2-yl)-butyric acid ethyl ester (85.5 g) was taken up in dry Et2O (50 mL). This mixture was added dropwise to a suspension of LiAlH4 (16.1 g) in dry Et2O (200 mL), cooled in an ice bath. The mixture was refluxed for 4 h., cooled in an ice bath, and quenched by adding H2O (16.1 mL), 2M aqueous NaOH (32.2 mL) and again H2O (16.1 mL). The suspension was filtered, the filter cake was washed with Et2O, and the combined filtrates were evaporated to dryness. The residue (49 g) was purified by vacuum distillation (112-125° C., 15 mbar), yielding 43.5 g of a clear, colorless liquid. 1H NMR (400 MHz, CDCl3) δ 0.98 (t, J=7.5 Hz, 3H), 1.10-1.24 (m, 1H), 1.31 (s, 3H), 1.50-1.75 (m, 2H), 3.12, (br s, 1H), 3.59-3.76 (m, 2H), 3.94-4.02 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728018B2
出典データセットuspto-grants-2010_06
ORD IDord-fcb3b7df7fec4410b638d2761073fb52
出典メモuspto-grants-2010_06