Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50565생성일: 2026년 10월 24일
Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → (E)-3-[4-(2-Pyridinyl)phenyl]-2-propenal
https://huagongshe.com/ko/reaction/50565
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- | HCID 112414 | — |
| 반응물 | 4-Pyridin-2-ylbenzaldehyde | HCID 1515240 | — |
| 반응물 | (1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide | HCID 2724194 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Potassium Carbonate | HCID 11430 | — |
| 생성물 | (E)-3-[4-(2-Pyridinyl)phenyl]-2-propenal | HCID 22630962 | 89% |
반응 단계
A mixture of 4-(2-pyridinyl)-benzaldehyde (1.76 g, 9.58 mmol), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (6.45 g, 15.02 mmol), and TDA-1 (Tris(3,6-dioxaheptyl)amine, 3.20 mL, 10.00 mmol) in dichloromethane (50 mL) and sat. aq. K2CO3 (50 mL) was heated to reflux for 20 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×25 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (MgSO4), and concentrated. THF (25 mL) and 10% HCl (25 mL) were added and the mixture was stirred for 1 h at rt. The reaction mixture was cooled to 0° C., made basic with 10% NaOH, and extracted with ethyl acetate (3×25 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (MgSO4), and concentrated. Purification by chromatography (SiO2, 3:1 hexane/ethyl acetate) provided 1.69 g (89%) of the title compound as a yellow solid. MS 210 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713455B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-bad2f943fd7c49719d72604fed49f6af |
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| 출처 메모 | uspto-grants-2004_03 |
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