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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1086993생성일: 2026년 10월 25일

Water → Methyl 2-(2-(benzyloxy)phenyl)-3-methoxyacrylate

https://huagongshe.com/reaction/1086993

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Dimethyl SulfateHCID 6497—
반응물Potassium CarbonateHCID 11430—
반응물Methyl 2-(2'-benzyloxyphenyl)-3-hydroxyacrylateHCID 69942437—
용매DimethylformamideHCID 6228—
생성물Methyl 2-(2-(benzyloxy)phenyl)-3-methoxyacrylateHCID 838698—
생성물Methyl 2-(2-(benzyloxy)phenyl)acetateHCID 11076055—

반응 단계

The crude methyl 3-hydroxy-2-(2'-benzyloxyphenyl)propenoate was dissolved in dry DMF (100 ml) and potassium carbonate (29.0 g) was added in one portion. Dimethyl sulphate (16.00 g) in dry DMF (10 ml) was then added dropwise with stirring. After ninety minutes, water (300 ml) was added and the solution was extracted with ether (2 x 300 ml). After washing with water (3 x 150 ml) and brine, the extracts were dried and concentrated under reduced pressure, and the resulting yellow oil solidified on trituration with ether/petrol. Recrystallization from dry methanol afforded E-methyl 3-methoxy-2-(2'-benzyloxyphenyl)propenoate as a white, crystalline solid (5.44g, 17% yield from methyl 2-benzyloxyphenylacetate), M.P. 76-77° C.; infrared maxima (nujol mull): 1710, 1640 cm-1 ; 1H nmr (CDCl3, 90MHz): delta 3.63 (3H,s), 3.75 (3H,s), 5.05 (2H,s), 6.80-7.40 (9H,m), 7.50 (1H,s)ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05034388
출처 데이터셋uspto-grants-1991_07
ORD IDord-a1c0d762440c4a9c8b15d14b0891577c
출처 메모uspto-grants-1991_07