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Water → 3-Hydroxy-4-phenylbenzylamine

HRID 2236462
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HRID 2236462 반응식
[N:1]([CH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[C:7]([O:17]C)[CH:6]=1)=[N+]=[N-].O.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[N-]=[N+]=[N-]>C1COCC1>[NH2:1][CH2:4][C:5]1[CH:6]=[C:7]([OH:17])[C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 11776TriphenylphosphineHCID 33558AzideHCID 593002734-Azidomethyl-2-methoxy-biphenyl

생성물 1

HCID 231438563-Hydroxy-4-phenylbenzylamine수율 100.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

4-Azidomethyl-2-methoxy-biphenyl (100 mg, 0.42 mmol) is dissolved in THF (5 mL) and H2O (0.5 mL) and to which PPh3 (100 mg, 0.38 mmol) is added. The mixture is allowed to stir at room temperature overnight. After analysis of TLC suggested the disappearance of the starting azide, the reaction is stopped and THF evaporated. The residue is purified through chromatography to provide the title compound (84 mg, 100%).

후처리

  1. customTHF evaporated
  2. customThe residue is purified through chromatography

출처 및 근거

ORD 기록
ord-c4ba39ed33d5439ab0a16394336b2f0b
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07713994B2

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