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HRID 594786作成日:2026年10月26日

3,5-Dimethoxybenzaldehyde → 4-(3,5-Dimethoxyphenyl)-3-butenoic acid

https://huagongshe.com/reaction/594786

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DimethoxybenzaldehydeHCID 81747—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物(2-Carboxyethyl)triphenylphosphonium bromideHCID 2733850—
溶媒TetrahydrofuranHCID 8028—
生成物4-(3,5-Dimethoxyphenyl)-3-butenoic acidHCID 8516724338.1%

反応条件

温度-78 °C

反応手順

To a solution of (2-carboxyethyl)triphenylphosphonium bromide (13.7 g, 33 mmol) in dry THF (50 mL) was added NaHMDS (33 mL, 66 mmol) dropwise at −20° C. under N2 and the reaction stirred for 20 min. The reaction was cooled to −78° C. and 3,5-dimethoxybenzaldehyde (5.0 g, 30 mmol) was added, and the reaction mixture stirred overnight while warming to rt. The reaction was quenched with water and extracted with EtOAc. The aqueous layer was acidified to pH=2 with dilute HCl solution and extracted with EtOAc again. The combined organic layers were washed with brine, dried (Na2SO4) and concentrated to give 2.54 g (38%) of the title compound as an orange gum. [M+H] Calc'd for C12H14O4, 223. Found, 223.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242968B2
出典データセットuspto-grants-2016_01
ORD IDord-7d5809919f2449e9b58f5810f1f4a2dc
出典メモuspto-grants-2016_01