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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (2-(Dimethylamino)ethyl)triphenylphosphonium bromide | HCID 2724136 | — |
| 반응물 | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| 반응물 | Methyl 3-(4-formylphenyl)-2-propenoate | HCID 53401287 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (E)-3-[4-(3-Dimethylaminopropenyl)phenyl]acrylic Acid | HCID 70098974 | 34% |
| 생성물 | (E)-3-[4-(3-dimethylaminopropenyl)phenyl]acrylic acid, methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06306870B1 |
|---|
| 출처 데이터셋 | uspto-grants-2001_10 |
|---|
| ORD ID | ord-a7a238b8d69a489785480e37eade0a0f |
|---|
| 출처 메모 | uspto-grants-2001_10 |
|---|