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

Trifluoroacetic acid → 2-(Benzamido)-4-(4-nitrophenyl)benzoic acid

HRID 1673457
노트
인쇄 미리보기

반응식

HRID 1673457 반응식
FC(F)(F)C(O)=O.[C:8]([NH:16][C:17]1[CH:29]=[C:28]([C:30]2[CH:35]=[CH:34][C:33]([N+:36]([O-:38])=[O:37])=[CH:32][CH:31]=2)[CH:27]=[CH:26][C:18]=1[C:19]([O:21]C(C)(C)C)=[O:20])(=[O:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>>[C:8]([NH:16][C:17]1[CH:29]=[C:28]([C:30]2[CH:35]=[CH:34][C:33]([N+:36]([O-:38])=[O:37])=[CH:32][CH:31]=2)[CH:27]=[CH:26][C:18]=1[C:19]([OH:21])=[O:20])(=[O:15])[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6422Trifluoroacetic acidHCID 67342488Tert-butyl 2-(benzamido)-4-(4-nitrophenyl)benzoate

생성물 1

HCID 578794682-(Benzamido)-4-(4-nitrophenyl)benzoic acid수율 43.3%

실험 절차

3.0 mL of trifluoroacetic acid solution containing 40 mg of tert-butyl 2-(benzamido)-4-(4-nitrophenyl)benzoate was stirred at room temperature for 1 hour. The solvent was evaporated under reduced pressure and ethyl acetate and methanol were added to she obtained residue and a solid substance was separated by filtration to obtain 15 mg of 2-(benzamido)-4-(4-nitrophenyl)benzoic acid as white solid.

후처리

  1. customThe solvent was evaporated under reduced pressure and ethyl acetate and methanol
  2. additionwere added to she
  3. custom
obtained residue
  • customa solid substance was separated by filtration
  • 출처 및 근거

    ORD 기록
    ord-24abcda32b684f88aa56d2d1895cf91e
    출처 데이터셋
    uspto-grants-2011_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07999132B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트