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

Nitric Acid → 5-Fluoro-2-methyl-1,3-dinitrobenzene

HRID 1416904
노트
인쇄 미리보기

반응식

HRID 1416904 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1.[N+:12]([O-])([OH:14])=[O:13]>S(=O)(=O)(O)O>[N+:12]([C:6]1[CH:7]=[C:2]([F:1])[CH:3]=[C:4]([N+:9]([O-:11])=[O:10])[C:5]=1[CH3:8])([O-:14])=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 679654-Fluoro-2-nitrotoluene

생성물 1

HCID 184653725-Fluoro-2-methyl-1,3-dinitrobenzene

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매2회

반응 조건

온도
2.5 °C

실험 절차

Fuming sulfuric acid (180 mL) is added dropwise to 4-fluoro-2-nitrotoluene (50.21 g) under an argon atmosphere. The internal temperature of the mixture is maintained at 0-5° C. using an ice/sodium chloride bath. A preformed (ice bath) mixture of fuming nitric acid (30 mL) and fuming sulfuric acid (90 mL) is added dropwise to the previous solution over three hours. The reaction is then allowed to warm to room temperature. After stirring at room temperature for 2 hours, the mixture is poured slowly into ice and the products are extracted with methylene chloride (4×500 mL). The combined extracts are dried over magnesium sulfate, filtered and rotary evaporated. The crude mixture is filtered through a short pad of silica gel, using 10% ethyl acetate/hexanes as solvent, then recrystallized from ethyl acetate/hexanes to afford 2,6-dinitro-4-fluorotoluene as a pale yellow solid.

후처리

  1. additionis added dropwise to the previous solution over three hours
  2. temperatureto warm to room temperature
  3. additionthe mixture is poured slowly into ice
  4. extractionthe products are extracted with methylene chloride (4×500 mL)
  5. dry with materialThe combined extracts are dried over magnesium sulfate
  6. filtrationfiltered
  7. filtrationThe crude mixture is filtered through a short pad of silica gel
  8. customrecrystallized from ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-72e04db3eb064587b1ed225eb7ba1cc6
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05916900

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트