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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 226276생성일: 2026년 10월 26일

4-Methyl hydrogen 2-methylenesuccinate → 4-Methoxy-3-methyl-4-oxobutanoic acid

https://huagongshe.com/reaction/226276

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl hydrogen 2-methylenesuccinateHCID 81791—
반응물(R)-4-Methoxy-2-methyl-4-oxobutanoic acidHCID 6398856—
반응물HCID 178418361HCID 178418361—
용매MethanolHCID 887—
생성물4-Methoxy-3-methyl-4-oxobutanoic acidHCID 13925570—

반응 조건

온도135 °C

반응 단계

133 mg (0.182 mmol) of (RophosARhCOD)CF3SO3 (=precatalyst) were introduced under protective gas into 21 ml of methanol in a 4 l (enamel) Pfaudler autoclave and 526 g (3-65 mol) of 2-methylenesuccinic acid 4-monomethyl ester (=substrate) dissolved in 704 ml of methanol were added. Hydrogenation was then carried out at 40° C. under 5 bar of hydrogen. Conversion of the substrate was complete after 4 h (1H-NMR, 500 MHz). The enantiomeric excess of the product (2R)-methylsuccinic acid 4-monomethyl ester was determined by gas chromatography to be >98% (from: BGB-Analytik, column type: BGB-174, length: 30 m, internal diameter: 0.25 ml, film thickness: 0.25 μm, carrier gas: helium, inlet pressure: 2.35 bar, temperature: 135° C., heating rate: 1.2° C./min, retention time of R enantiomer: 23.3 min, retention time of S enantiomer: 22.6 min). The s/c ratio was 20 000:1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557240B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-6800811c6ca04a96994e956cc3e6a28b
출처 메모uspto-grants-2009_07