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Tert-butyl 2-(benzamido)-4-(2-fluorophenyl)benzoate → 2-(Benzamido)-4-(2-fluorophenyl)benzoic acid

HRID 1673471
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인쇄 미리보기

반응식

HRID 1673471 반응식
[C:1]([NH:9][C:10]1[CH:22]=[C:21]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[F:29])[CH:20]=[CH:19][C:11]=1[C:12]([O:14]C(C)(C)C)=[O:13])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>FC(F)(F)C(O)=O>[C:1]([NH:9][C:10]1[CH:22]=[C:21]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[F:29])[CH:20]=[CH:19][C:11]=1[C:12]([OH:14])=[O:13])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 67343885Tert-butyl 2-(benzamido)-4-(2-fluorophenyl)benzoate

생성물 1

HCID 578796152-(Benzamido)-4-(2-fluorophenyl)benzoic acid

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

10 mL of trifluoroacetic acid was added to the obtained tert-butyl 2-(benzamido)-4-(2-fluorophenyl)benzoate and stirred at room temperature for 2 hours. The solvent was evaporated under reduced pressure and toluene was added. The solvent was evaporated under reduced pressure and diisopropyl ether was added to the obtained residue and a solid substance was separated by filtration to obtain 93 mg of 2-(benzamido)-4-(2-fluorophenyl)benzoic acid as white solid.

후처리

  1. customThe solvent was evaporated under reduced pressure and toluene
  • additionwas added
  • customThe solvent was evaporated under reduced pressure and diisopropyl ether
  • additionwas added to the obtained residue
  • customa solid substance was separated by filtration
  • 출처 및 근거

    ORD 기록
    ord-491096f8d0d744cdb03eee7af5063fb8
    출처 데이터셋
    uspto-grants-2011_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07999132B2

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