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

Oxalic Acid → 6,7-Bis(trifluoromethyl)-1,4-dihydroquinoxaline-2,3-dione

HRID 53809
노트
인쇄 미리보기

반응식

HRID 53809 반응식
[F:1][C:2]([F:16])([F:15])[C:3]1[C:8]([C:9]([F:12])([F:11])[F:10])=[CH:7][C:6]([NH2:13])=[C:5]([NH2:14])[CH:4]=1.[C:17](O)(=[O:21])[C:18](O)=[O:19]>Cl>[F:1][C:2]([F:15])([F:16])[C:3]1[CH:4]=[C:5]2[C:6](=[CH:7][C:8]=1[C:9]([F:12])([F:11])[F:10])[NH:13][C:18](=[O:19])[C:17](=[O:21])[NH:14]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 971Oxalic AcidHCID 40613654,5-Bis(trifluoromethyl)benzene-1,2-diamine

생성물 1

HCID 211900176,7-Bis(trifluoromethyl)-1,4-dihydroquinoxaline-2,3-dione수율 35.1%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A mixture of 102 mg (0.418 mmol) of 4,5-bis(trifluoromethyl)-1,2-phenylenediamine and 37 mg (0.411 mmol) of oxalic acid in 2 mL of 2N HCl was refluxed for 6 h and cooled to room temperature. The mixture was filtered and washed by water, CHCl3 and dried to leave a colorless solid (43 mg, 35%), mp >250° C. 1H NMR (DMSO-d6), 7.629 (s, 2) 12.293 (s, 2). 19F NMR (DMSO-d6), 62.185 (s).

후처리

  1. temperaturewas refluxed for 6 h
  2. filtrationThe mixture was filtered
  3. washwashed by water, CHCl3
  4. customdried

출처 및 근거

ORD 기록
ord-c443c11ddcb64bd0a6e62fcc14512a15
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05620979

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트