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Triphenylphosphine → HCID 18383984, 화합물

HRID 2297732
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HRID 2297732 반응식
[CH:1]#[C:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].I[C:10]1[CH:11]=[C:12]([CH:15]=[CH:16][C:17]=1[O:18][CH2:19][O:20][CH3:21])[CH:13]=[O:14].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(Cl)Cl.[Cu](I)I.C([O-])(=O)C.C([O-])(=O)C.[Pd+2]>[C:1]([C:10]1[CH:11]=[C:12]([CH:15]=[CH:16][C:17]=1[O:18][CH2:19][O:20][CH3:21])[CH:13]=[O:14])#[C:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 11776TriphenylphosphineHCID 123701-OctyneHCID 10402059Benzaldehyde, 3-iodo-4-(methoxymethoxy)-

생성물 1

HCID 18383984HCID 18383984, 화합물수율 45.2%

시약·촉매·용매 3

HCID 83717Copper iodide촉매HCID 167845palladium(II) acetate
촉매
HCID 6344Dichloromethane용매

실험 절차

Under an argon atmosphere, copper iodide (190 mg, 1.0 mmol), 1-octyne (0.55 mL, 5.0 mmol) and 3-iodo-4-methoxymethoxybenzaldehyde (291 mg, 1.0 mmol) were added to a solution (2 mL) of palladium (II) diacetate (11 mg, 0.05 mmol) and triphenylphosphine (52 mg, 0.20 mmol) in methylene chloride, followed by stirring at room temperature for 2 hours. Next, the reaction solution was filtered through celite, and the solvent contained in the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluted with ethyl acetate/hexane=1/10) to give 3-(1-octyn-1-yl)-4-methoxymethoxybenzaldehyde (124 mg, yield 45%).

후처리

  1. filtrationNext, the reaction solution was filtered through celite
  2. customwas evaporated under reduced pressure
  3. customThe residue was purified by silica gel column chromatography (eluted with ethyl acetate/hexane=1/10)

출처 및 근거

ORD 기록
ord-b2f9cf1afa254210951bad91ae577cd5
출처 데이터셋
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06492392B1

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