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

Cyclopropylamine → 7-Hydroxyindole

HRID 439395
노트
인쇄 미리보기

반응식

HRID 439395 반응식
[NH:1]1[C:9]2[C:4](=[CH:5]C=CC=2)[C:3](=[O:10])[CH2:2]1.[CH:11]1(N)[CH2:13][CH2:12]1>C1(C)C=CC=CC=1.[Ti](Cl)(Cl)(Cl)Cl>[NH:1]1[C:2]2[C:13](=[CH:12][CH:5]=[CH:4][C:3]=2[OH:10])[CH:11]=[CH:9]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 69828CyclopropylamineHCID 2309151,2-dihydro-3H-indol-3-one

생성물 1

HCID 27376517-Hydroxyindole

시약·촉매·용매 2

HCID 24193Titanium Tetrachloride촉매HCID 1140Toluene용매2회

반응 조건

온도
-10 °C

실험 절차

7-Chloroacetyloxy-1,4-dihydro-4-methylcyclopent b!indol-3(2H)-one (15.0 g) and cyclopropylamine (9.6 g) were dissolved in 300 ml toluene and cooled to -10° C. Titanium tetrachloride (6.3 g) dissolved in 50 ml toluene was added slowly to the first solution. The reaction mixture was allowed to come up to room temperature and stirred overnight. The next day another 1.5 equivalents of the amine (4.6 g) was added to the reaction mixture and the mixture was stirred for one hour. The reaction mixture was filtered through a pad of silica gel, eluting with 3:1 hexane/ethyl acetate, giving a yellow oil after removal of solvents. 3-Cyclopropylamino-4-methyl-1,2,3,4-tetrahydrocyclopent b!-indol-7-ol was isolated as a light yellow solid (3.3 g) after flash chromatography and recrystallization from ethyl acetate.

후처리

  1. additionwas added slowly to the first solution
  2. customto come up to room temperature
  3. stirringthe mixture was stirred for one hour
  4. filtrationThe reaction mixture was filtered through a pad of silica gel
  5. washeluting with 3:1 hexane/ethyl acetate
  6. customgiving a yellow oil
  7. customafter removal of solvents

출처 및 근거

ORD 기록
ord-752619c4d85e4a9cad4738d3192ff18b
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05514700

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트