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

Dichloromethane → Methyl 2,6-dichloro-4-nitrobenzoate

HRID 24711
노트
인쇄 미리보기

반응식

HRID 24711 반응식
[Cl:1][C:2]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[C:7]([Cl:14])[C:3]=1[C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH2:19](Cl)Cl>>[Cl:1][C:2]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[C:7]([Cl:14])[C:3]=1[C:4]([O:6][CH3:19])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6344DichloromethaneHCID 24386Thionyl ChlorideHCID 225719382,6-Dichloro-4-nitrobenzoic acid

생성물 1

HCID 22571909Methyl 2,6-dichloro-4-nitrobenzoate수율 80%

실험 절차

To 2,6-dichloro-4-nitrobenzoic acid (12.8 g, U.S. Pat. No. 3,423,475) was added anhydrous CH2Cl2 (60 mL) and thionyl chloride (40 mL) then the resulting mixture was refluxed for 19 h. The mixture was allowed to cool to room temperature and evaporated. Additional CH2Cl2 (10 mL) was added and the solution was evaporated. MeOH (100 mL) was added to the residue and the mixture was refluxed for 17 h. The mixture was allowed to cool to room temperature and placed in an ice-bath. The precipitated solid was collected by filtration to give methyl 2,6-dichloro-4-nitrobenzoate (10.8 g, 80%).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. temperaturethe resulting mixture was refluxed for 19 h
  2. customevaporated
  3. additionAdditional CH2Cl2 (10 mL) was added
  4. customthe solution was evaporated
  5. additionMeOH (100 mL) was added to the residue
  6. temperaturethe mixture was refluxed for 17 h
  7. temperatureto cool to room temperature
  8. customplaced in an ice-bath
  9. filtrationThe precipitated solid was collected by filtration

출처 및 근거

ORD 기록
ord-6d762d0e226b43b2b3aba6015f88fd43
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06855843B2

반응 노트

불러오는 중…