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HRID 33986作成日:2026年10月24日

Water → Methyl 4-(4-formyl-2-methoxyphenoxy)butanoate

https://huagongshe.com/ja/reaction/33986

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物VanillinHCID 1183—
反応物Potassium CarbonateHCID 11430—
反応物Methyl 4-bromobutyrateHCID 107604—
溶媒DimethylformamideHCID 6228—
生成物Methyl 4-(4-formyl-2-methoxyphenoxy)butanoateHCID 1075329166%

反応手順

A solution of vanillin (47)(40.00 g, 262.89 mmol) and methyl-4-bromobutyrate (50.00 g, 276.18 mmol) in DMF (200 mL) was allowed to stir over potassium carbonate (51.53 g, 372.40 mmol) for 16 hours. Water was added to the reaction mixture at which time the product crystallised. The resulting mixture was filtered and dried in vacuo for 16 hours to afford the keto-ester (48) as a white solid (41.3 g, 66%). MP=57-59° C. 1H NMR (250 MHz, CDCl3) δ 9.80 (s, 1H), 7.46-7.40 (m, 2H), 6.97 (d, J=8.1 Hz, 1H), 4.16 (t, J=6.3 Hz, 2H), 3.92 (s, 3H), 3.70 (s, 3H), 2.57 (t, J=7.2 Hz, 2H), 2.20 (pent, J=6.7 Hz, 2H). 13C NMR (67.8 MHz, CDCl3) 188.2 (Cl), 173.7 (C12), 153.8 (Cquat.), 152.0 (Cquat.), 144.1 (Cquat.), 125.8 (Cmethine), 110.3 (C3), 108.5 (C6), 69.0 (C9), 57.0 (C8), 52.2 (C13), 30.6 (C11), 24.5 (C10). It was decided to adopt the numbering system shown in the figure below for the molecule for ease of peak assignment in 13C NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429658B2
出典データセットuspto-grants-2008_09
ORD IDord-44a5e748fd264f4bbf8f4ac6744d97fd
出典メモuspto-grants-2008_09