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HRID 322848作成日:2026年10月26日

Water → (E)-3-(2,4-dibenzyloxyphenyl)prop-2-enoic acid

https://huagongshe.com/reaction/322848

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2,4-Bis(benzyloxy)benzaldehydeHCID 1809080—
反応物Diethyl phosphonoacetic acidHCID 17786294—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(E)-3-(2,4-dibenzyloxyphenyl)prop-2-enoic acidHCID 1073723436.7%

反応条件

温度-70 °C

反応手順

To a solution of 2.5 M n-butyl lithium (3.64 mL) in dry tetrahydrofuran (THF) (20 mL) that is cooled to −70° C. under nitrogen is added a solution of diethyl phosphonoacetic acid (0.89 g) in THF (5 mL). After 30 minutes a solution of 2,4-dibenzyloxybenzaldehyde (1.46 g) in THF (5 mL) is slowly added to the cooled solution so as to maintain the temperature. The resulting mixture is stirred at −70° C. for 3 hours and then at 25° C. for 18 hours. The resulting suspension is treated with water, the THF is removed in vacuo,the residue is extracted with ethyl acetate, the extract is dried and evaporated. The residual solid is recrystallized from isopropanol to yield (E)-3-(2,4-dibenzyloxyphenyl)prop-2-enoic acid as colourless crystals (0.6 g), m.p. 153-155° C. H NMR (DMSO) 5.15 (2H,s), 5.21(2H,s), 6.4(1H,d,J=16 Hz), 6.7(1H,d), 6.85(1H,s), 7.3-7.5(10H,m), 7.6(1H,d), 7.8(1H,d,J=16 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211234B1
出典データセットuspto-grants-2001_04
ORD IDord-633593c12a7d4fa1bd1831ffcea2d9aa
出典メモuspto-grants-2001_04