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

Water → HCID 178419467, 화합물

HRID 1614167
노트
인쇄 미리보기

반응식

HRID 1614167 반응식
[Br:1][C:2]1[C:3](O)=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.O.[NH2:14][NH2:15].Cl.Cl.NN.O>C(O)CO>[Br:1][C:2]1[C:3]([NH:4][C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)=[N:14][NH:15][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 17548Hydrazine, dihydrochlorideHCID 24654Hydrazine hydrate (1:1)HCID 178517115HCID 178517115, 화합물

생성물 1

HCID 178419467HCID 178419467, 화합물

시약·촉매·용매 1

HCID 174Ethylene Glycol용매

실험 절차

The bromohydroxyquinoline (1.97 g, 8.79 mmol) was dissolved in 21 ml of ethylene glycol and hydrazine hydrate (4.2 ml) was added. To this mixture were added 1.3 g (12.2 mmol) of hydrazine dihydrochloride, and the resulting mixture was heated to reflux and stirred under nitrogen. The resulting material was poured onto 300 ml of H2O. The mixture was extracted with CH2Cl2, basified with NaHCO and extracted further with CH2Cl2. The combined organic portions were washed with water, dried over Na2SO4, filtered, and concentrated in vacuo to give a brown oil, yielding bromoanilinopyrazole (i.e., 3-(2-amino-5-bromophenyl)pyrazole).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperaturethe resulting mixture was heated
  2. temperatureto reflux
  3. extractionThe mixture was extracted with CH2Cl2
  4. extractionextracted further with CH2Cl2
  5. washThe combined organic portions were washed with water
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customto give a brown oil

출처 및 근거

ORD 기록
ord-f7725d41b44846c2b010858af37be6ff
출처 데이터셋
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05196421

반응 노트

불러오는 중…