Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1056528생성일: 2026년 10월 27일
Acetic Acid → (Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylate
https://huagongshe.com/reaction/1056528
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Glycinamide hydrochloride | HCID 2723639 | — |
| 반응물 | Ethyl 3-(2-(2-hydroxyethoxy)phenyl)-3-oxopropanoate | HCID 86684692 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (Z)-Ethyl 3-((2-amino-2-oxoethyl)amino)-3-(2-(2-hydroxyethoxy)phenyl)acrylate | HCID 86684693 | — |
반응 단계
To a solution of ethyl 3-(2-(2-hydroxyethoxy)phenyl)-3-oxopropanoate (2 g, 7.94 mmol) and glycinamide hydrochloride (3.5 g, 31.7 mmol) in methanol (20 mL) was added triethylamine (3.21 g, 31.7 mmol) at room temperature. The mixture was stirred at 40° C. for 20 min. Acetic acid (1.9 g, 31.7 mmol) was added, and the mixture was stirred at 80° C. for 18 hours. The reaction mixture was cooled to room temperature and saturated sodium bicarbonate (200 mL) was added. The organic layer was separated, dried (Na2SO4) and concentrated to give a yellow solid. The solid was washed with EtOAc (20 mL), and the residue was dried under reduced pressure to give the title compound as a white solid. This material was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09399626B2 |
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| 출처 데이터셋 | uspto-grants-2016_07 |
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| ORD ID | ord-29e44ddd688143d58849177165f2ba68 |
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| 출처 메모 | uspto-grants-2016_07 |
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