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

Ethyl 2-ethoxy-5-[(4-methylpiperazin-1-yl)sulfonyl]benzoate → 2-Ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)benzaldehyde

HRID 1581739
노트
인쇄 미리보기

반응식

HRID 1581739 반응식
[CH2:1]([O:3][C:4]1[CH:14]=[CH:13][C:12]([S:15]([N:18]2[CH2:23][CH2:22][N:21]([CH3:24])[CH2:20][CH2:19]2)(=[O:17])=[O:16])=[CH:11][C:5]=1[C:6](OCC)=[O:7])[CH3:2]>O=[Mn]=O>[CH2:1]([O:3][C:4]1[CH:14]=[CH:13][C:12]([S:15]([N:18]2[CH2:23][CH2:22][N:21]([CH3:24])[CH2:20][CH2:19]2)(=[O:16])=[O:17])=[CH:11][C:5]=1[CH:6]=[O:7])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 22052241Ethyl 2-ethoxy-5-[(4-methylpiperazin-1-yl)sulfonyl]benzoate

생성물 1

HCID 98397652-Ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)benzaldehyde수율 47.4%

시약·촉매·용매 1

HCID 14801Manganese dioxide촉매

실험 절차

MnO2 (100 g, 1.15 mol) was loaded into a flask, followed by 1-(4-ethoxy-3-hydroxymethylphenylsulfonyl)-4-methylpiperazine (15 g, 0.05 mol, from step (b) above). This was washed with acetone (150 mL) and the suspension stirred for 3 hours. The MnO2 was filtered off onto Celite® and the filtrate concentrated under vacuum to give a pale yellow oil. This was recrystallised from toluene to give the title compound as a pale green solid (7.4 g, 47%).

후처리

  • washThis was washed with acetone (150 mL)
  • filtrationThe MnO2 was filtered off onto Celite®
  • concentrationthe filtrate concentrated under vacuum
  • customto give a pale yellow oil
  • customThis was recrystallised from toluene
  • 출처 및 근거

    ORD 기록
    ord-d3196747ca41476fafde0a110ee2bd5b
    출처 데이터셋
    uspto-grants-2004_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06730786B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트