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

Bromine → 3,3-Bis-fluoromethyl-1-bromo-1-(4-chlorophenoxy)-butan-2-one

HRID 2198765
노트
인쇄 미리보기

반응식

HRID 2198765 반응식
[F:1][CH2:2][C:3]([CH2:16][F:17])([CH3:15])[C:4](=[O:14])[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=1.[Br:18]Br>C(Cl)Cl>[F:1][CH2:2][C:3]([CH2:16][F:17])([CH3:15])[C:4](=[O:14])[CH:5]([Br:18])[O:6][C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24408BromineHCID 130194353,3-Bisfluoromethyl-1-(4-chlorophenoxy)-butan-2-one

생성물 1

HCID 130194363,3-Bis-fluoromethyl-1-bromo-1-(4-chlorophenoxy)-butan-2-one수율 89%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

166 g (0.632 mol) of 3,3-bisfluoromethyl-1-(4-chlorophenoxy)-butan-2-one were dissolved in 500 ml of methylene chloride, and 100 g (0.625 mol) of bromine were added dropwise at 20° to 30° C., while stirring and cooling. The mixture was subsequently stirred at 20° C. for 2 hours. After distilling off the solvent in vacuo, the residue was crystallized from petroleum ether. 190 g (88% of theory) of 3,3-bisfluoromethyl-1-bromo-1-(4-chlorophenoxy)-butan-2-one of melting point 54°-57° C. were obtained. ##STR75##

후처리

  1. temperaturecooling
  2. stirringThe mixture was subsequently stirred at 20° C. for 2 hours
  3. distillationAfter distilling off the solvent in vacuo
  4. customthe residue was crystallized from petroleum ether

출처 및 근거

ORD 기록
ord-9a198ae3d32b4e0290c40276e29d9607
출처 데이터셋
uspto-grants-1982_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04359470

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트