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

Chlorine → 2,6-Dichloropyridin-3-ol

HRID 1833827
노트
인쇄 미리보기

반응식

HRID 1833827 반응식
[Cl:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][N:3]=1.[Cl:9]Cl>CN(C)C=O>[Cl:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[C:4]([Cl:9])[N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24526ChlorineHCID 811362-Chloro-3-pyridinol

생성물 1

HCID 1043172,6-Dichloropyridin-3-ol

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
20 °C

실험 절차

100 g (0.77 mole) of 2-chloro-3-pyridinol is dissolved in 350 ml of dimethylformamide. In the course of 1.5 hours, 70 ml of chlorine (measured at -80°; 0.93 mole) is introduced at 0° into the stirred solution. The reaction mixture is subsequently stirred for 1.5 hours at 20° C and afterwards concentrated in a rotary evaporator (bath: 50°; 10 torr). To the residue are added 400 ml of water and 100 ml of ether. The two phases are separated, and the aqueous phase is extracted 5 times with 100 ml of ether each time. The combined ether phases are washed with water and dried. The solvent is removed in vacuo; the semisolid residue is stirred with 1.6 liters of water, and the resulting suspension is adjusted to pH 3. The suspension is heated to boiling, and after a few minutes the solution is decanted from an oily residue. The solution is purified with active charcoal, and the yellow product, obtained on cooling, is recrystallised from water; m.p. 136°-138° C; yield: 42 g;

후처리

  1. concentrationafterwards concentrated in a rotary evaporator (bath: 50°; 10 torr)
  2. additionTo the residue are added 400 ml of water and 100 ml of ether
  3. customThe two phases are separated
  4. extractionthe aqueous phase is extracted 5 times with 100 ml of ether each time
  5. washThe combined ether phases are washed with water
  6. customdried
  7. customThe solvent is removed in vacuo
  8. stirringthe semisolid residue is stirred with 1.6 liters of water
  9. temperatureThe suspension is heated
  10. customafter a few minutes the solution is decanted from an oily residue
  11. customThe solution is purified with active charcoal
  12. customthe yellow product, obtained
  13. temperatureon cooling
  14. customis recrystallised from water

출처 및 근거

ORD 기록
ord-f19df750125a4912b7de39ae688d0715
출처 데이터셋
uspto-grants-1978_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04067725

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트