Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1488254생성일: 2026년 10월 27일
Potassium Carbonate → 2,2'-[(2-{[3-(Benzyloxy)-3-oxopropyl]amino}-2-oxoethyl)imino]diacetic acid
https://huagongshe.com/reaction/1488254
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2,6-dioxo-N-(carboxymethyl)morpholine | HCID 169531 | — |
| 반응물 | Benzyl 3-aminopropanoate hydrochloride | HCID 19434764 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2,2'-[(2-{[3-(Benzyloxy)-3-oxopropyl]amino}-2-oxoethyl)imino]diacetic acid | HCID 117996360 | — |
반응 단계
To an ice bath cooled solution of benzyl 3-aminopropanoate hydrochloride (4.49 g, 20.8 mmol) in DMF (30 mL) was added K2CO3 (3.02 g, 21.84 mmol) and the resulting mixture was stirred at o° C. for 2 hr. The mixture was then filtered and the filtrate was added to an ice bath cooled solution of 2-(2,6-dioxomorpholino)acetic acid (4.47 g, 25.8 mmol) in DMF (30 mL). The resulting mixture was stirred at 0° C. for 30 min, then at rt for 2 hr. The reaction was quenched by the addition of water (30 mL) and the resulting mixture was concentrated. The residue was stirred with water (40 mL), and the resulting precipitate was collected through filtration and dried to give the title compound. 1H NMR (DMSO-d6) δ 2.53 (t, J=6.8, 2H), 3.27 (s, 2H), 3.36 (q, J=6.2, 2H), 3.42 (m, m 2H), 3.49 (s, 2H), 5.09 (s, 2H), 7.28 (m, 4H), 8.16 (m, 1H), 12.45 (br s, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09427475B2 |
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| 출처 데이터셋 | uspto-grants-2016_08 |
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| ORD ID | ord-017ba17c0fc54d9ab0d8a33f5cfce7fa |
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| 출처 메모 | uspto-grants-2016_08 |
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