돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1532832생성일: 2026년 10월 25일

Methyl morpholine oxide → 4-Formyl-2-phenylbenzoyl methionine methyl ester

https://huagongshe.com/reaction/1532832

반응식

참여 물질

역할이름HCID투입량
반응물Methyl morpholine oxideHCID 82029—
반응물4,4,6-Trimethyl-2-vinyl-1,3,2-dioxaborinaneHCID 107310—
반응물(2-Phenyl4bromobenzoyl)-methionine methyl esterHCID 20622824—
촉매Osmium TetroxideHCID 30318—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Sodium CarbonateHCID 10340—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물4-Formyl-2-phenylbenzoyl methionine methyl esterHCID 10571267—

반응 조건

온도25 °C

반응 단계

A mixture of (2-phenyl-4-bromobenzoyl) methionine methyl ester (100 mmol), 4,4,6-trimethyl-2-vinyl-1,3,2-dioxaborinane (100 mmol), tetrakis(triphenylphosphine)palladium (0) (3 mmol) in toluene and 2 M sodium carbonate in water (100 mL) is heated at 80° C. until the starting methyl ester disappears. The resulting mixture is extracted with ether, and washed with water, brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue is then purified by column chromatography on silica gel. To a solution of the resulting vinyl compound in dioxane/water (4/1) is added osmium tetraoxide (0.03 equivalent), N-methylmorpholine N-oxide (3 equivalents), and the reaction is stirred at 25° C. until TLC analysis shows the reaction to be complete. The reaction mixture is extracted with ether, which is washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue is then purified by column chromatography on silica gel to afford the title product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06204293B1
출처 데이터셋uspto-grants-2001_03
ORD IDord-64d87d992617438cbbffe0767df052a0
출처 메모uspto-grants-2001_03