戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 83578作成日:2026年10月26日

2-Methyl-2-butene → 3-(2,4-Dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic Acid

https://huagongshe.com/reaction/83578

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-buteneHCID 10553—
反応物Sodium ChloriteHCID 23668197—
反応物Sodium Phosphate, Monobasic, DihydrateHCID 23673460—
反応物3-(2,4-Dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carbaldehydeHCID 86680389—
溶媒WaterHCID 962—
溶媒t-Butanol tetrahydrofuran waterHCID 22124471—
生成物3-(2,4-Dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic AcidHCID 8668039032.4%

反応条件

温度0 °C

反応手順

Under argon atmosphere, to a solution of 3-(2,4-dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carbaldehyde (10.8 mg) in tert-butanol/tetrahydrofuran/water (4/3/1, 0.5 ml) was added sodium dihydrogenphosphate dihydrate (20.2 mg) at room temperature. This reaction mixture was cooled to 0° C., 2-methyl-2-butene (18 μl) and sodium chlorite (9.0 mg) were sequentially added thereto, and then the mixture was stirred at room temperature for 24 hours. This reaction mixture was cooled to 0° C., and then water was added thereto, and the mixture was extracted with ethyl acetate. This organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel thin-layer chromatography (eluent: chloroform/methanol=9/1) to give the titled compound (3.7 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846746B2
出典データセットuspto-grants-2014_09
ORD IDord-0c337cdeb8dc458b94b46fd9137580fc
出典メモuspto-grants-2014_09