戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 381484作成日:2026年10月26日

(2-(Dimethylamino)ethyl)triphenylphosphonium bromide → (E)-3-[4-(3-Dimethylaminopropenyl)phenyl]acrylic Acid

https://huagongshe.com/reaction/381484

反応式

関与物質

役割名称HCID仕込み量
反応物(2-(Dimethylamino)ethyl)triphenylphosphonium bromideHCID 2724136—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物Methyl 3-(4-formylphenyl)-2-propenoateHCID 53401287—
溶媒DimethylformamideHCID 6228—
生成物(E)-3-[4-(3-Dimethylaminopropenyl)phenyl]acrylic AcidHCID 7009897434%
生成物(E)-3-[4-(3-dimethylaminopropenyl)phenyl]acrylic acid, methyl esterHCID 86755260—

反応手順

(E)-3-[4-(3-Dimethylaminopropenyl)phenyl]acrylic acid, methyl ester was prepared by the following way: (2-dimethylaminoethyl)triphenylphosphonium bromide (7.2 g, 17.4 mmol) in 30 mL of DMF was treated with KHMDS (27 mL, 1.01 equiv., 0.5 M in toluene) at −78° C. for one hour. At −40° C., 3-(4-formylphenyl)acrylic acid, methyl ester (2.54 g, 13.3 mmol, prepared according to the procedure of Syper, L.; Miochowski, J. Synthesis, 1984, 9, 747-752) was added dropwise. The resulting mixture was stirred for 12 hours at rt and quenched with water. Extraction with EtOAc, drying over MgSO4 and evaporation in vacuo gave a residue that was purified via flash chromatography with DCM:MeOH (90:10) as eluting solvent. The title compound (1.1 g, 34%) was obtained as an orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06306870B1
出典データセットuspto-grants-2001_10
ORD IDord-a7a238b8d69a489785480e37eade0a0f
出典メモuspto-grants-2001_10