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Benzaldehyde → 2,4-Di(prop-1-en-2-yl)dibenzo[b,d]thiophen-3-amine

HRID 1750926
ノート
印刷プレビュー

反応式

HRID 1750926 の反応式
Br[C:2]1[C:14]([NH2:15])=[C:13](Br)[C:5]2[S:6][C:7]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[C:4]=2[CH:3]=1.[CH3:17][C:18]1(C)[C:22](C)(C)OB(C(C)=C)O1.[CH:29](=O)[C:30]1C=CC=C[CH:31]=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>C(OCC)(=O)C.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].O.C1(C)C=CC=CC=1>[CH2:17]=[C:18]([C:2]1[C:14]([NH2:15])=[C:13]([C:30]([CH3:31])=[CH2:29])[C:5]2[S:6][C:7]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[C:4]=2[CH:3]=1)[CH3:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 240BenzaldehydeHCID 62657Potassium Phosphate, TribasicHCID 109974264,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 584010402,4-Dibromodibenzo[b,d]thiophen-3-amine

生成物 1

HCID 584009962,4-Di(prop-1-en-2-yl)dibenzo[b,d]thiophen-3-amine収率 95%

試薬・触媒・溶媒 4

HCID 9811564
Bis(dibenzylideneacetone)palladium
触媒
HCID 962Water溶媒
HCID 1140Toluene溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

To a degassed toluene (200 mL), 2,4-dibromodibenzo[b,d]thiophen-3-amine (12.15 g, 34.0 mmol), 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (17.15 g, 102 mmol), benzaldehyde (3.61 g, 34.0 mmol), potassium phosphate (23.51 g, 102 mmol) dicyclohexyl(2′,6′-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine (1.676 g, 4.08 mmol) and Pd2(dba)3 (0.935 g, 1.021 mmol) and water (20 mL) were sequentially added. The solution was refluxed for overnight in an atmosphere of nitrogen and then allowed to cool to room temperature. The reaction was diluted with ethyl acetate and the organic phase was separated from the aqueous phase. The organic phase was dried over sodium sulfate and the solvent was removed under vacuum. The product was chromatographed using silica gel with ethylacetate and hexanes as the eluent. The solvent was removed to give the title compound (9.0, 95%).

後処理

  1. temperatureThe solution was refluxed for overnight in an atmosphere of nitrogen
  2. customthe organic phase was separated from the aqueous phase
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. customthe solvent was removed under vacuum
  5. customThe product was chromatographed
  6. customThe solvent was removed

出典と根拠

ORDレコード
ord-03171f66983c42f68f9f6cbdfa382131
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09156870B2

反応ノート

読み込み中…

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