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HRID 1450156作成日:2026年10月26日

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

https://huagongshe.com/reaction/1450156

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Dimethyl SulfateHCID 6497—
反応物Potassium CarbonateHCID 11430—
反応物Methyl 2-(2'-benzyloxyphenyl)-3-hydroxyacrylateHCID 69942437—
溶媒DimethylformamideHCID 6228—
生成物Methyl 2-(2-(benzyloxy)phenyl)-3-methoxyacrylateHCID 838698—
生成物Methyl 2-(2-(benzyloxy)phenyl)acetateHCID 11076055—

反応手順

The crude methyl 2-(2'-benzyloxyphenyl)-3-hydroxyacrylate 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 (2×300 ml). After washing with water (3×150 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 2-(2'-benzyloxyphenyl) -3-methoxyacrylate as a white, crystalline solid (5.44 g, 17% yield from methyl 2-benzyloxyphenylacetate), mp. 76-77° C.; infrared max. (nujol mull): 1710, 1640 cm-1 ; 1H nmr (90 MHz): delta 3.63 (3H, s), 3.75 (3H, s), 5.05 (2H,s), 6.80-7.40 (9H,m), 7.50 (1H,s)ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05602076
出典データセットuspto-grants-1997_02
ORD IDord-39baa328488a4f06a95cf95f93db7760
出典メモuspto-grants-1997_02