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

Methanol → Methyl 3-bromo-6-chloropicolinate

HRID 2208803
노트
인쇄 미리보기

반응식

HRID 2208803 반응식
[Br:1][C:2]1[C:3]([C:9]([OH:11])=[O:10])=[N:4][C:5]([Cl:8])=[CH:6][CH:7]=1.OS(O)(=O)=O.[CH3:17]O>>[Br:1][C:2]1[C:3]([C:9]([O:11][CH3:17])=[O:10])=[N:4][C:5]([Cl:8])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 269667323-Bromo-6-chloropyridine-2-carboxylic acid

생성물 1

HCID 46311200Methyl 3-bromo-6-chloropicolinate수율 93%

실험 절차

To a stirred solution of 3-bromo-6-chloropyridine-2-carboxylic acid (2.00 g, 8.46 mmol) in MeOH (40 ml) was added H2SO4 (189 μl, 3.55 mmol) and the solution was heated to reflux for 16 h. The reaction was cooled and the MeOH removed under reduced pressure, the resulting solid was dissolved in EtOAc (100 ml) and washed with saturated NaHCO3 solution (2×50 ml) followed by brine (50 ml), dried (Na2SO4) and evaporated under reduced pressure to afford the title compound as an off-white solid (1.97 g, 93%) which was used without any further purification. LC-MS 98%, m/z=249.8/251.7/253.7

후처리

  1. temperaturethe solution was heated
  2. temperatureto reflux for 16 h
  3. temperatureThe reaction was cooled
  4. customthe MeOH removed under reduced pressure
  5. dissolutionthe resulting solid was dissolved in EtOAc (100 ml)
  6. washwashed with saturated NaHCO3 solution (2×50 ml)
  7. dry with materialdried (Na2SO4)
  8. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-079fa3a6aacc450da6aa46cf1b2f89a7
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09376422B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트