Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl Acetate → 3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | Benzyl 2-methyl-1-oxa-5-azaspiro[2.4]heptane-5-carboxylate | HCID 21041146 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl ester | HCID 69068640 | — |
반응 단계
A solution of 2-methyl-1-oxa-5-azaspiro[2,4]heptane-5-carboxylic acid benzyl ester (Example A9, 0.31 g, 1.25 mmol) in methanol (10 mL) and ammonium hydroxide (7 mL) is heated in a sealed tube at 100° C. for 16 hours. After cooling, the reaction mixture is dissolved ethyl acetate, washed with water, dried over Na2SO4 and evaporated to afford the title compound (0.340 g). 1H NMR (200 MHz, CDCl3): δ 7.33-7.26 (m, 5H), 5.28 (bs, 2H), 5.07 (s, 2H), 3.56-3.16 (m, 5H), 2.03-1.76 (m, 2H), 1.15 (d, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07582627B2 |
| 출처 데이터셋 | uspto-grants-2009_09 |
| ORD ID | ord-7c80a79c95894e24811c18acb38497b1 |
| 출처 메모 | uspto-grants-2009_09 |