Toluene → 2-Phenyl-5-(prop-1-en-2-yl)pyridine
反応式
Cl[C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[N:6][CH:7]=1.O.[O-]P([O-])([O-])=O.[K+].[K+].[K+].[C:23]1(C)[CH:28]=CC=C[CH:24]=1.CC1(C)C(C)(C)OB(C(C)=C)O1>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].C1(P(C2CCCCC2)C2C=CC=CC=2C2C(OC)=CC=CC=2OC)CCCCC1.O>[C:8]1([C:5]2[CH:4]=[CH:3][C:2]([C:23]([CH3:28])=[CH2:24])=[CH:7][N:6]=2)[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
To a 1 L round bottom flask was added 5-chloro-2-phenylpyridine (10.15 g, 53.5 mmol), dicyclohexyl(2′,6′-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine (1.8 g, 4.3 mmol), potassium phosphate tribasic monohydrate (37.0 g, 161 mmol) with toluene (200 mL) and water (20 mL). The reaction mixture was degassed with nitrogen for 20 mins. 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (12.07 mL, 64.2 mmol) and Pd2(dba)3 (0.980 g, 1.070 mmol) were added and the reaction mixture was refluxed for 18 h. The aqueous layer was removed and the organic layer was concentrated to dryness. The crude product was chromatographed on silica gel with 0-20% EtOAc in hexane to yield 11 g of the desired product (HPLC purity: 95%). The product was confirmed by GC/MS.
後処理
- customThe reaction mixture was degassed with nitrogen for 20 mins
- temperaturethe reaction mixture was refluxed for 18 h
- customThe aqueous layer was removed
- concentrationthe organic layer was concentrated to dryness
- customThe crude product was chromatographed on silica gel with 0-20% EtOAc in hexane
出典と根拠
- ORDレコード
- ord-271642aac05f4487b44d3be4ea80f09f
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08709615B2
反応ノート
読み込み中…