홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Phthalic Anhydride → Ethyl 2-(1,3-dioxoisoindol-2-yl)propanoate

HRID 1713393
노트
인쇄 미리보기

반응식

HRID 1713393 반응식
[C:1]1(=[O:11])[O:6][C:4](=O)[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[NH2:12][CH:13]([CH3:19])[C:14]([O:16][CH2:17][CH3:18])=[O:15]>C1CCCCC1>[O:11]=[C:1]1[C:2]2[C:3](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4](=[O:6])[N:12]1[CH:13]([CH3:19])[C:14]([O:16][CH2:17][CH3:18])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6811Phthalic AnhydrideHCID 69236NoName_3047

생성물 1

HCID 305258Ethyl 2-(1,3-dioxoisoindol-2-yl)propanoate수율 89%

시약·촉매·용매 1

HCID 8078Cyclohexane용매

실험 절차

20.87 g (0.141 mol) of phthalic anhydride together with 16.5 g (0.141 mol) of ethyl aminopropionate in an open round-bottom flask at 120° C. for 5 h. 300 ml of cyclohexane are added, and the mixture is heated to reflux. The hot cyclohexane solution is decanted off from the remaining oil and completely concentrated. A slowly solidifying viscous oil is obtained (31 g, 89% yield).

후처리

  1. temperaturethe mixture is heated to reflux
  2. customThe hot cyclohexane solution is decanted off from the remaining oil
  3. concentrationcompletely concentrated
  4. customis obtained (31 g, 89% yield)

출처 및 근거

ORD 기록
ord-1401872a989446519dd536cd0dce47fe
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07795278B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트