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

Carbon Tetrachloride → 1-Trichloromethyl-3,4-dinitrobenzene

HRID 903090
노트
인쇄 미리보기

반응식

HRID 903090 반응식
[N+:1]([C:4]1[CH:5]=[C:6](C)[CH:7]=[CH:8][C:9]=1[N+:10]([O-:12])=[O:11])([O-:3])=[O:2].O(Cl)Cl.[C:17]([Cl:21])(Cl)([Cl:19])[Cl:18]>>[Cl:18][C:17]([Cl:21])([Cl:19])[C:6]1[CH:7]=[CH:8][C:9]([N+:10]([O-:12])=[O:11])=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 5943Carbon TetrachlorideHCID 118833,4-DinitrotolueneHCID 24646Chlorine monoxide

생성물 1

HCID 233376401-Trichloromethyl-3,4-dinitrobenzene수율 96%

실험 절차

3,4-Dinitrotoluene (2.49 g 0.0136 mole) and dichlorine monoxide (4.74 g, 0.055 mole) in carbon tetrachloride (50 ml) were heated in a Carrius tube from which air had been removed, as in Example 6 at 75° for 10 hrs. The reaction solution was filtered to remove a white solid (0.35 g) which was identified by its infrared spectra as 3,4-dinitrobenzoic acid. The filtrate was dried (MgSO4) and the solvent removed on a rotary evaporator to give 1-trichloromethyl-3,4-dinitrobenzene as a white crystalline solid (3.57 g, purity by HPLC 96% yield 89.2%). The product was recrystallized from carbon tetrachloride-petroleum ether to give essentially pure product (mp 69.5°-70.6°).

후처리

  1. customhad been removed, as in Example 6 at 75° for 10 hrs
  2. filtrationThe reaction solution was filtered
  3. customto remove a white solid (0.35 g) which
  4. dry with materialThe filtrate was dried (MgSO4)
  5. customthe solvent removed on a rotary evaporator

출처 및 근거

ORD 기록
ord-6b67a031a42344ae85aa557f7617c73f
출처 데이터셋
uspto-grants-1980_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04226783

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트