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4-Pentyn-1-ol → 5-[1-(4-Trimethylsilanylethynyl-phenyl)-1H-indol-5-yl]-pent-4-yn-1-ol

HRID 1633663
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HRID 1633663 반응식
[CH3:1][Si:2]([C:5]#[C:6][C:7]1[CH:12]=[CH:11][C:10]([N:13]2[C:21]3[C:16](=[CH:17][C:18](OS(C(F)(F)F)(=O)=O)=[CH:19][CH:20]=3)[CH:15]=[CH:14]2)=[CH:9][CH:8]=1)([CH3:4])[CH3:3].[CH2:30]([OH:35])[CH2:31][CH2:32][C:33]#[CH:34]>N1CCCCC1.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Cu]I>[CH3:3][Si:2]([C:5]#[C:6][C:7]1[CH:8]=[CH:9][C:10]([N:13]2[C:21]3[C:16](=[CH:17][C:18]([C:34]#[C:33][CH2:32][CH2:31][CH2:30][OH:35])=[CH:19][CH:20]=3)[CH:15]=[CH:14]2)=[CH:11][CH:12]=1)([CH3:4])[CH3:1]
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참가 물질

6

반응물 2

HCID 793464-Pentyn-1-olHCID 86585591Trifluoro-methanesulfonic acid 1-(4-trimethylsilanylethynyl-phenyl)-1H-indol-5-yl ester

생성물 1

HCID 186794765-[1-(4-Trimethylsilanylethynyl-phenyl)-1H-indol-5-yl]-pent-4-yn-1-ol수율 71.3%

시약·촉매·용매 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매
HCID 11979704
Tetrakis(triphenylphosphine)palladium
촉매
HCID 8082Piperidine용매

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온도
80 °C

실험 절차

To 1.62 g (3.7 mmol) Trifluoro-methanesulfonic acid 1-(4-trimethylsilanylethynyl-phenyl)-1H-indol-5-yl ester in 5 ml piperidine, 230 mg (0.2 mmol) tetrakis-(triphenylphosphine)-palladium and 40 mg (0.2 mmol) CuI were added. The solution was evaporated and purged with argon three times, before 0.56 ml (6 mmol) 4-pentyn-1-ol were added. The solution was stirred at 80° C. for 2 h. The solution was concentrated and the residue dissolved in 0.5M HCl and ether. The inorganic phase was extracted with ether, the organic phases were washed with water and dried over Na2SO4. Purification on silica gel with CH2Cl2 yielded 980 mg (71%) 5-[1-(4-Trimethylsilanylethynyl-phenyl)-1H-indol-5-yl]-pent-4-yn-1-ol as orange viscous oil, MS: 371 (M).

후처리

  1. customThe solution was evaporated
  2. additionwere added
  3. concentrationThe solution was concentrated
  4. dissolutionthe residue dissolved in 0.5M HCl
  5. extractionThe inorganic phase was extracted with ether
  6. washthe organic phases were washed with water
  7. dry with materialdried over Na2SO4
  8. customPurification on silica gel with CH2Cl2

출처 및 근거

ORD 기록
ord-f7f57941906c4b52887534cd90ccc342
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06503907B2

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