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

Nitric Acid → 4-(Methylsulfanyl)-2-nitrophenol

HRID 1587805
노트
인쇄 미리보기

반응식

HRID 1587805 반응식
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1.[N+:10]([O-])([OH:12])=[O:11]>C(Cl)Cl>[N+:10]([C:7]1[CH:8]=[C:3]([S:2][CH3:1])[CH:4]=[CH:5][C:6]=1[OH:9])([O-:12])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 140864-(Methylthio)phenol

생성물 1

HCID 187958574-(Methylsulfanyl)-2-nitrophenol

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 4-(methylthio)phenol(5.0 g) in methylene chloride (100 mls) was added 30% nitric acid absorbed on silica (9.29 g) and the mixture stirred at room temperature for 3 hrs. The mixture was filtered and washed with methylene chloride. The solvent was evaporated and the residue was purified by flash chromatography eluting with ethyl acetate and hexane (15:85 v/v) to give 2-nitro-4-(methylthio)phenol as an orange solid (2.22 g); NMR (200 MHz, CDCl3): 2.50(3H,s), 7.10(1H,d,J=8 Hz), 7.51(1H,dd,J=8 Hz), 7.95(1H,d,J=3 Hz).

후처리

  1. customabsorbed on silica (9.29 g)
  2. filtrationThe mixture was filtered
  3. washwashed with methylene chloride
  4. customThe solvent was evaporated
  5. customthe residue was purified by flash chromatography
  6. washeluting with ethyl acetate and hexane (15:85 v/v)

출처 및 근거

ORD 기록
ord-527709443e6f4d37a1d5b9b8914c479d
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05219874

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트