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Quinoline → HCID 10419313, 화합물

HRID 971839
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HRID 971839 반응식
[CH3:1][Si:2]([CH3:9])([CH3:8])[C:3]#[C:4][CH:5]([OH:7])[CH3:6].N1C2C(=CC=CC=2)C=CC=1.[H][H]>[Pd].C1C=CC=CC=1>[CH3:1][Si:2]([CH3:9])([CH3:8])/[CH:3]=[CH:4]\[CH:5]([OH:7])[CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 7047QuinolineHCID 27608284-(Trimethylsilyl)but-3-yn-2-olHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 10419313HCID 10419313, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 241Benzene용매

실험 절차

A solution of 94.15 parts by weight of 4-(trimethylsilyl)-3-butyn-2-ol (II) in 940 parts by volume of benzene and 4.7 parts by volume of quinoline is hydrogenated at a constant pressure of 2 p.s.i. in the presence of 9.4 parts by weight of 5% palladium on barium sulfate until one equivalent of hydrogen is consumed. The catalyst is removed and the solution is washed twice with 100 parts per volume of 5% aqueous hydrochloric acid and then with water. After drying over sodium sulfate, the solvent is removed and the residue is distilled at 33°-39° C./0.3 mm to give cis-4-(trimethylsilyl)-3-buten-2-ol (III) which has the following structural formula: ##STR9##

후처리

  1. customThe catalyst is removed
  2. washthe solution is washed twice with 100 parts per volume of 5% aqueous hydrochloric acid
  3. dry with materialAfter drying over sodium sulfate
  4. customthe solvent is removed
  5. distillationthe residue is distilled at 33°-39° C./0.3 mm

출처 및 근거

ORD 기록
ord-afb8b828a19f49ac893cc2572d30c87a
출처 데이터셋
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04161480

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