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HCID 9967439, 화합물 → 1-(3-Carboxy-4-hydroxyphenyl)-2-phenylindole

HRID 1579867
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HRID 1579867 반응식
[C:1]([C:4]1[CH:5]=[C:6]([N:11]2[C:19]3[CH2:18][CH2:17][CH2:16][CH2:15][C:14]=3[CH:13]=[C:12]2[C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:7]=[CH:8][C:9]=1[OH:10])([OH:3])=[O:2]>[Pd].C1(C)C(C)=CC=CC=1>[C:1]([C:4]1[CH:5]=[C:6]([N:11]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[CH:13]=[C:12]2[C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:7]=[CH:8][C:9]=1[OH:10])([OH:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 9967439HCID 9967439, 화합물

생성물 1

HCID 122703211-(3-Carboxy-4-hydroxyphenyl)-2-phenylindole

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 7237O-Xylene용매

실험 절차

A mixture of 3.33 g. (0.01 mole) of 1-(3-carboxy-4-hydroxyphenyl)-2-phenyl-4,5,6,7-tetrahydroindole, 4.0 g. of 10% palladium on carbon, and 250 ml. of xylene was heated under reflux with stirring under nitrogen for 3 days, filtered, and concentrated to a solid. Trituration with cyclohexane afforded 2.4 g. (73%) of solid, m.p. 210°-212°. Recrystallization from acetic acid gave colorless crystals, m.p. 213.5°-214.5°.

후처리

  • additionA mixture of 3.33 g
  • temperatureunder reflux
  • filtrationfiltered
  • concentrationconcentrated to a solid
  • customTrituration with cyclohexane afforded 2.4 g
  • customRecrystallization from acetic acid
  • customgave colorless crystals, m.p. 213.5°-214.5°
  • 출처 및 근거

    ORD 기록
    ord-728bd90c54ec400d846fa60fc1d7adc7
    출처 데이터셋
    uspto-grants-1976_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US03931407

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