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

Trifluoromethanesulfonic acid → 1-Chloro-2,5-difluoro-4-iodobenzene

HRID 1480580
노트
인쇄 미리보기

반응식

HRID 1480580 반응식
FC(F)(F)S(O)(=O)=O.[Cl:9][C:10]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:11]=1[F:17].[I:18]N1C(=O)CCC1=O>>[Cl:9][C:10]1[CH:15]=[C:14]([F:16])[C:13]([I:18])=[CH:12][C:11]=1[F:17]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 62406Trifluoromethanesulfonic acidHCID 120273N-IodosuccinimideHCID 1375611-Chloro-2,5-difluorobenzene

생성물 1

HCID 510000881-Chloro-2,5-difluoro-4-iodobenzene수율 77.5%

반응 조건

온도
0 °C

실험 절차

Trifluoromethanesulfonic acid (9.9 mL, 110 mmol) was added to 2-chloro-1,4-difluorobenzene (2.2 g, 15 mmol) at room temperature and then cooled to 0° C. N-Iodosuccinimide (3.16 g, 14.1 mmol) was then added in multiple portions. After 10 minutes, the reaction mixture was allowed to warm to room temperature and stirred for 2 hours. The reaction mixture was poured over ice-water and extracted with hexane. The organic layer was washed with saturated Na2SO4, dried and concentrated. The crude product was purified by silica gel chromatography (100% hexanes) to give 1-chloro-2,5-difluoro-4-iodobenzene (3.0 g, 74%). 1H NMR (400 MHz, CDCl3) δ 7.52 (dd, J=5.4, 7.8, 1H), 7.17-7.08 (m, 1H).

후처리

  1. temperatureto warm to room temperature
  2. extractionextracted with hexane
  3. washThe organic layer was washed with saturated Na2SO4
  4. customdried
  5. concentrationconcentrated
  6. customThe crude product was purified by silica gel chromatography (100% hexanes)

출처 및 근거

ORD 기록
ord-c6bb46bd04d54b9da2a0f0fbc0b9de59
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409886B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트