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

Iodine → 2-Iodo-4-(trifluoromethyl)phenol

HRID 22733
노트
인쇄 미리보기

반응식

HRID 22733 반응식
[I:1]I.C(=O)(O)[O-].[Na+].[F:8][C:9]([F:18])([F:17])[C:10]1[CH:11]=[CH:12][C:13]([OH:16])=[CH:14][CH:15]=1.NC(N)=S>C1COCC1.O>[F:8][C:9]([F:17])([F:18])[C:10]1[CH:11]=[C:12]([I:1])[C:13]([OH:16])=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 807IodineHCID 678744-(Trifluoromethyl)phenolHCID 516892Sodium BicarbonateHCID 2723790Thiourea

생성물 1

HCID 115728162-Iodo-4-(trifluoromethyl)phenol

시약·촉매·용매 2

HCID 962Water용매HCID 8028
Tetrahydrofuran
용매

실험 절차

A mixture of iodine (91.6 mmol, 23.2 g) and sodium bicarbonate (91.6 mmol, 7.7 g) was added to a solution of α,α,α-trifluoro-p-cresol (83.3 mmol, 13.5 g) in THF (90 mL) and H2O (90 mL) and the reaction mixture was allowed to stand at room temperature overnight. Sufficient thiourea (5% solution) was added to remove the excess iodine as indicated by the color change of the reaction from deep violet to brown. The reaction mixture was extracted with ether (3×100 mL), the extract was dried, filtered and the filtrate was concentrated to obtain a brown oil. This oil was distilled (bp 105° C. at 44 mm Hg) to obtain α,α,α-trifluoro-o-iodo-p-cresol (4.1 g, 75% pure, admixed with the starting α,α,α-trifluoro-p-cresol).

후처리

  1. customto remove the excess iodine
  2. customas indicated by the color change of the reaction from deep violet to brown
  3. extractionThe reaction mixture was extracted with ether (3×100 mL)
  4. customthe extract was dried
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated
  7. customto obtain a brown oil
  8. distillationThis oil was distilled (bp 105° C. at 44 mm Hg)

출처 및 근거

ORD 기록
ord-272e7eff9e6b4c39bef402449fd68506
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06849629B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트