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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83578생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/83578

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-buteneHCID 10553—
반응물Sodium ChloriteHCID 23668197—
반응물Sodium Phosphate, Monobasic, DihydrateHCID 23673460—
반응물3-(2,4-Dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carbaldehydeHCID 86680389—
용매WaterHCID 962—
용매t-Butanol tetrahydrofuran waterHCID 22124471—
생성물3-(2,4-Dimethoxybenzyl)-4-oxo-3-azabicyclo[3.1.0]hexane-1-carboxylic AcidHCID 8668039032.4%

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846746B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0c337cdeb8dc458b94b46fd9137580fc
출처 메모uspto-grants-2014_09