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Diethylamine → 4-(4-Propylphenyl)-4'-(1-propynyl)tolan

HRID 465890
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HRID 465890 반응식
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][CH3:17])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1)#[CH:2].[C:18]([C:21]1[CH:26]=[CH:25][C:24](I)=[CH:23][CH:22]=1)#[C:19]C.[CH2:28](NCC)C>[Cu](I)I>[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([C:15]#[C:16][C:17]3[CH:23]=[CH:22][C:21]([C:26]#[C:25][CH3:24])=[CH:18][CH:19]=3)=[CH:11][CH:10]=2)=[CH:5][CH:4]=1)[CH2:2][CH3:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8021DiethylamineHCID 121767134-(1-Propynyl)iodobenzeneHCID 198149114-Ethynyl-4'-propyl-1,1'-biphenyl

생성물 1

HCID 867461894-(4-Propylphenyl)-4'-(1-propynyl)tolan

시약·촉매·용매 1

HCID 83717Copper iodide촉매

실험 절차

4-Ethynyl-4'-propylbiphenyl (prepared according to the method disclosed in Japanese patent application laid-open No. Sho 58-110527/1983) (2.2 g, 0.01 mol) and 4-(1-propynyl)iodobenzene (2.4 g, 0.01 mol) were dissolved in diethylamine (20 ml), and then copper iodide (0.11 g, 0.15 mmol) and dichlorobistriphenylphosphinepalladium dichloride (0.21 g, 0.3 mmol) were added. The resulting mixture was subjected to reaction and purification operation in the same manner as in Example 1, to obtain the objective 4-(4-propylphenyl)-4'-(1-propynyl)tolan (compound

후처리

  1. customThe resulting mixture was subjected to reaction and purification operation in the same manner as in Example 1

출처 및 근거

ORD 기록
ord-3bde6962d55944a9a8362f04d41b31f7
출처 데이터셋
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05154851

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