Tri(butyl)vinyltin → 1-(2-Methyl-4-nitrophenyl)-3-vinylpyridin-2(1H)-one

HRID 218513ノート

反応式

HRID 218513 の反応式
Br[C:2]1[C:3](=[O:18])[N:4]([C:8]2[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][C:9]=2[CH3:17])[CH:5]=[CH:6][CH:7]=1.[CH2:19](C([Sn])=C(CCCC)CCCC)[CH2:20]CC>O1CCOCC1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:17][C:9]1[CH:10]=[C:11]([N+:14]([O-:16])=[O:15])[CH:12]=[CH:13][C:8]=1[N:4]1[CH:5]=[CH:6][CH:7]=[C:2]([CH:19]=[CH2:20])[C:3]1=[O:18]

参加物

5

反応物 2

HCID 53438229Tri(butyl)vinyltinHCID 594101573-Bromo-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-one

生成物 1

HCID 594101981-(2-Methyl-4-nitrophenyl)-3-vinylpyridin-2(1H)-one

試薬・触媒・溶媒 2

HCID 178418397HCID 178418397、化合物触媒HCID 312751,4-Dioxane溶媒

実験手順

50 g (162 mmol) of the compound from example 41A are dissolved in 700 ml of anhydrous dioxane and admixed with 62 g (194 mmol) of tributylvinyltin and 4.7 g (4.0 mmol) of tetrakis(triphenylphosphine)palladium, and the mixture is heated at reflux for 15 h. It is allowed to cool and filtered through kieselguhr. It is washed with ethyl acetate, and the combined filtrates are concentrated to dryness under reduced pressure. The residue is applied to silica gel and chromatographed on 800 g of silica gel with a gradient of cyclohexane and ethyl acetate. This affords 27 g (62% of theory) of the desired product.

後処理

  1. temperaturethe mixture is heated
  2. temperatureat reflux for 15 h
  3. temperatureto cool
  4. filtrationfiltered through kieselguhr
  5. washIt is washed with ethyl acetate
  6. concentrationthe combined filtrates are concentrated to dryness under reduced pressure
  7. customchromatographed on 800 g of silica gel with a gradient of cyclohexane and ethyl acetate

出典と根拠

ORDレコード
ord-1ce46bb10fc0475cb1a816ef8e29b722
出典データセット
uspto-grants-2012_06
特許番号
US08198267B2

反応ノート

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