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HRID 392816作成日:2026年10月24日

Imidazole → HCID 23519143、化合物

https://huagongshe.com/ja/reaction/392816

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物L-Malic AcidHCID 222656—
反応物(S)-2-(2,2-Dimethyl-5-oxo-1,3-dioxolan-4-yl)acetic acidHCID 641720—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物HCID 23519143HCID 2351914396%

反応条件

温度22 °C

反応手順

A solution of (S)-(+)-2,2-dimethyl-5-oxo-1,3-dioxolane-4-acetic acid (13.20 g, 75.8 mmol), which was derived from L-malic acid by means known in the art, in N,N-dimethylformamide (25 ml) was treated at 22° C. with imidazole (10.56 g, 0.155 mmol) followed by tert-butyldimethylsilyl chloride (12.0 g, 79.6 mmol) and the resulting mixture was stirred at 22° C. for 18 h. The reaction mixture was then diluted with toluene (500 ml), washed with water (×3), saturated sodium bicarbonate and brine. After drying (magnesium sulfate), the solvent was evaporated under reduced pressure to give an oil. Distillation under vacuum gave 20.9 g (96%) of the title material as a clear oil: Bp 80-90° C./0.1 torr (bulb to bulb distillation, air bath temperature). 1H NMR (400 MHz, CDCl3) δ: 0.33 (s, 3), 0.36 (s, 3), 1.00 (s, 9), 1.11 (s, 3), 1.37 (s, 3), 2.72 (m, 2), 4.35 (dd, 1, J=4, 6).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06803378B2
出典データセットuspto-grants-2004_10
ORD IDord-085abdfc11834705b2a45f83d0e990f5
出典メモuspto-grants-2004_10