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

8-(2-Methoxyethoxy)quinoline → 1,2,3,4-Tetrahydro-8-methoxyethoxyquinoline

HRID 279974
노트
인쇄 미리보기

반응식

HRID 279974 반응식
[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:15]=1[N:14]=[CH:13][CH:12]=[CH:11]2>CO.O=[Pt]=O>[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:15]=1[NH:14][CH2:13][CH2:12][CH2:11]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 540377188-(2-Methoxyethoxy)quinoline

생성물 1

HCID 233230551,2,3,4-Tetrahydro-8-methoxyethoxyquinoline

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 887Methanol용매

실험 절차

8-Methoxyethoxyquinoline (6.48 g, 31.9 mmol) was dissolved in methanol (50 ml) and reduced on a Parr hydrogenation apparatus using PtO2 catalyst. The catalyst was removed, and the solution was taken to dryness. The dark brown oil which remained was purified on a short silica gel column using 4:1 heptane:ethyl acetate for elution. The isolated oil (1,2,3,4-tetrahydro-8-methoxyethoxyquinoline) had the following NMR spectrum: (CDCl3) δ 1.93 (quintet, 2, CH2 (beta-H)), 2.76 (tr, 2, CH2), 3.32 (tr, 2, CH2), 3.43 (s, 3, OMe), 3.72 (tr, 2, OCH2), 4.11 (tr, 2, CH2O), 4.31 (br, 1, NH), 6.57 (s, +sh, 3, Ar-3H). Anal. Calcd. for C12H17NO2 : C, 69.54; H, 8.27; N, 6.76. Found: C, 69.42; H, 8.26; N, 6.70.

후처리

  1. customThe catalyst was removed
  2. customThe dark brown oil which remained was purified on a short silica gel column
  3. washethyl acetate for elution

출처 및 근거

ORD 기록
ord-7a9cd8a51b0e46b084096ed0914052f1
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04587341

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트