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HRID 1270690作成日:2026年10月27日

Hydroxyphenylacetic acid → 3-(3,5-Dimethoxyphenyl)-2-(4-hydroxyphenyl)-acrylic acid

https://huagongshe.com/reaction/1270690

反応式

関与物質

役割名称HCID仕込み量
反応物Hydroxyphenylacetic acidHCID 127—
反応物Hydrochloric AcidHCID 313—
反応物Acetic AnhydrideHCID 7918—
反応物3,5-DimethoxybenzaldehydeHCID 81747—
溶媒TriethylamineHCID 8471—
生成物3-(3,5-Dimethoxyphenyl)-2-(4-hydroxyphenyl)-acrylic acidHCID 356751—

反応手順

To a mixture of 3,5-dimethoxybenzaldehyde (500 g, 3 mol) and p-hydroxyphenyl acetic acid (457 g, 3 mol) was added acetic anhydride (1 L) and triethylamine (420 mL). This non-homogeneous mixture on heating becomes homogeneous at ˜70° C. After being stirred at 130–140° C. for 6 h, the mixture was cooled to room temperature. Concentrated HCl (1 L) was added to the reaction mixture slowly in 50 min keeping temp between 20–30° C. The light yellow precipitate obtained was filtered and rinsed with Dl water in the Buchner funnel. The solid was dissolved in 3N NaOH (5 L ) and stirred for 1 h and filtered. The filtrate was acidified, maintaining a temperature at 25–30° C., with conc. HCl to pH 1. The precipitated product was filtered and washed with water to give crude product. The crude product was recrystallized from MeOH-H2O then dried at 40° C. for 6 h. Yield: pale yellow solid 428 g (47%). 1HNMR (DMSO-d6): δ12.48 (br, 1H), 9.42 (s, 1H), 7.59 (s, 1H), 6.95 (d, J=8.0 Hz, 2H), 6.76 (d, J=8.0 Hz, 2H), 6.35 (t, J=2.2 Hz, 1H), 6.27 (d, J=2.2 Hz, 2H), 3.56 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07202366B2
出典データセットuspto-grants-2007_04
ORD IDord-da40e2a9ef1345edbb1cfd72e6e84a65
出典メモuspto-grants-2007_04