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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 381484생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/381484

반응식

참여 물질

역할이름HCID투입량
반응물(2-(Dimethylamino)ethyl)triphenylphosphonium bromideHCID 2724136—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물Methyl 3-(4-formylphenyl)-2-propenoateHCID 53401287—
용매DimethylformamideHCID 6228—
생성물(E)-3-[4-(3-Dimethylaminopropenyl)phenyl]acrylic AcidHCID 7009897434%
생성물(E)-3-[4-(3-dimethylaminopropenyl)phenyl]acrylic acid, methyl esterHCID 86755260—

반응 단계

(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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06306870B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-a7a238b8d69a489785480e37eade0a0f
출처 메모uspto-grants-2001_10