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2-Amino-4-phenylphenol → HCID 22064189, 화합물

HRID 1827896
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HRID 1827896 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:5]=[CH:4][C:3]=1[OH:14].[Cl:15][CH2:16][C:17](OC)(OC)OC>>[Cl:15][CH2:16][C:17]1[O:14][C:3]2[CH:4]=[CH:5][C:6]([C:8]3[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=3)=[CH:7][C:2]=2[N:1]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 145622-Amino-4-phenylphenolHCID 1447021,1,1-Trimethoxy-2-chloroethane

생성물 1

HCID 22064189HCID 22064189, 화합물

반응 조건

온도
160 °C

실험 절차

2-amino-4-phenylphenol (0.180 g, 0.97 mmol) was placed in a Smith Process Vial™ (Personal Chemistry, Inc., Uppsala) (3 mL glass vessel) followed by the addition of 1-chloro-2,2,2-trimethoxyethane (1 mL). The vial was sealed and the mixture was heated in the Emrys Optimizer™ (Personal Chemistry, Inc., Uppsala) microwave at 160° C. for 300 s, fixed hold time on, absorption level normal, pre-stirring 10 s. It was then cooled to room temperature, diluted with 2 mL of methanol and purified by semi-prep HPLC. The HPLC fractions were evaporated under reduced pressure to furnish 2-(chloromethyl)-5-phenyl-benzoxazole as an off-white solid.

후처리

  1. custom
The vial was sealed
  • customabsorption level normal
  • temperatureIt was then cooled to room temperature
  • additiondiluted with 2 mL of methanol
  • custompurified by semi-prep HPLC
  • customThe HPLC fractions were evaporated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-f193044562254a25978d71b924c37984
    출처 데이터셋
    uspto-grants-2006_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07056924B2

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