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3-Butyn-1-OL → HCID 15475334, 화합물

HRID 566237
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HRID 566237 반응식
[C:1]1([C:7]([N:20]=[N+:21]=[N-:22])([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:23]([OH:27])[CH2:24][C:25]#[CH:26]>C1(C)C=CC=CC=1>[C:1]1([C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[N:20]2[CH:26]=[C:25]([CH2:24][CH2:23][OH:27])[N:22]=[N:21]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 135663-Butyn-1-OLHCID 84340Benzene, 1,1',1''-(azidomethylidyne)tris-

생성물 1

HCID 15475334HCID 15475334, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

In toluene (90 ml) were dissolved triphenylmethyl azide (8.23 g) and 3-butyn-1-ol (2.2 ml). The solution was heated for 60 hours under reflux. The reaction mixture was concentrated under reduced pressure. The concentrate was purified by means of a column chromatography (carrier: silica gel, 150 g, developing solvent: ethyl acetate). The resulting crystalline product was washed with isopropyl ether to give the title compound (3.06 g).

후처리

  • temperatureThe solution was heated for 60 hours
  • temperatureunder reflux
  • concentrationThe reaction mixture was concentrated under reduced pressure
  • customThe concentrate was purified by means of a column chromatography (carrier: silica gel, 150 g, developing solvent: ethyl acetate)
  • washThe resulting crystalline product was washed with isopropyl ether
  • 출처 및 근거

    ORD 기록
    ord-8cb29b10ee6e44eca7e8bc1d9d8cd25c
    출처 데이터셋
    uspto-grants-2001_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06174877B1

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