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

Potassium Nitrate → 1-Bromo-5-fluoro-2-methyl-4-nitrobenzene

HRID 1897661
노트
인쇄 미리보기

반응식

HRID 1897661 반응식
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH3:9].[N+:10]([O-])([O-:12])=[O:11].[K+]>S(=O)(=O)(O)O.O>[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([N+:10]([O-:12])=[O:11])=[CH:4][C:3]=1[CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24434Potassium NitrateHCID 740162-Bromo-4-fluorotoluene

생성물 1

HCID 534032861-Bromo-5-fluoro-2-methyl-4-nitrobenzene

시약·촉매·용매 2

HCID 962Water용매HCID 1118Sulfuric Acid용매2회

반응 조건

온도
0 °C

실험 절차

To a solution of 2-bromo-4-fluoro-1-methylbenzene (5 g, 26.4 mmol) dissolved in conc. sulfuric acid (20 mL) was added potassium nitrate (2.67 g, 26.4 mmol) in sulfuric acid (5 mL) at 0° C. After stirring at 0° C. for 1 hr, the reaction was diluted with water, extracted with ethyl acetate (3×40 mL). The combined organic phases were washed with saturated sodium bicarbonate solution and brine sequentially, and then dried over Na2SO4. The crude product obtained after concentration was purified by silica gel column chromatography with mixed solvent hexanes/EtOAc (95/5) to afford 1-bromo-5-fluoro-2-methyl-4-nitrobenzene as an orange solid. 1H NMR (400 MHz, chloroform-d) δ 7.93 (d, 1H, J=7.6 Hz), 7.50 (d, 1H, J=10 Hz), 2.43 (s, 3H).

후처리

  1. extractionextracted with ethyl acetate (3×40 mL)
  2. washThe combined organic phases were washed with saturated sodium bicarbonate solution and brine sequentially
  3. dry with materialdried over Na2SO4
  4. customThe crude product obtained
  5. concentrationafter concentration
  6. customwas purified by silica gel column chromatography with mixed solvent hexanes/EtOAc (95/5)

출처 및 근거

ORD 기록
ord-7dedfc3fba4f401d8f6a5f97b0b3dde6
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08519129B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트