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Ethyl Acrylate → 3-(6-Chloro-pyridin-3-yl)-acrylic acid ethyl ester

HRID 2376027
ノート
印刷プレビュー

反応式

HRID 2376027 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5](I)=[CH:4][N:3]=1.C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.C(N(C(C)C)CC)(C)C.[C:40]([O:44][CH2:45][CH3:46])(=[O:43])[CH:41]=[CH2:42]>CN(C=O)C.CCCCCC.CCOC(C)=O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O>[Cl:1][C:2]1[N:3]=[CH:4][C:5](/[CH:42]=[CH:41]/[C:40]([O:44][CH2:45][CH3:46])=[O:43])=[CH:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

10

反応物 4

HCID 8821Ethyl AcrylateHCID 80271Tri-o-tolylphosphineHCID 81531DiisopropylethylamineHCID 43971762-Chloro-5-iodopyridine

生成物 1

HCID 108461873-(6-Chloro-pyridin-3-yl)-acrylic acid ethyl ester

試薬・触媒・溶媒 5

HCID 167845palladium(II) acetate触媒
HCID 962
Water
溶媒
HCID 6228Dimethylformamide溶媒
HCID 8058Hexane溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
100 °C

実験手順

To a solution of 2-chloro-5-iodopyridine (37.7 g) in DMF (300 mL) was added palladium(II) acetate (1.77 g), tri-o-tolylphosphine (7.19 g), diisopropylethylamine (82 mL), and ethyl acrylate (17.9 mL), and the mixture was heated at 100° C. for 10 hours. Resulting mixture was poured into water and extracted with AcOEt. The organic layer was washed with water and brine and dried over Na2SO4, and the solvent was removed in vacuo. Obtained brown solid was suspended in a mixture of hexane and AcOEt (4:1), and the precipitate was filtered off. The filtrate was concentrated in vacuo, and residual brown oil was purified by silica gel column chromatography eluted with AcOEt and hexane (1:4-1:2). Resulting solid was triturated with IPE to give ethyl (2E)-3-(6-chloro-3-pyridyl)acrylate as pale yellow powder (20.58 g).

後処理

  1. customResulting mixture
  2. extractionextracted with AcOEt
  3. washThe organic layer was washed with water and brine
  4. dry with materialdried over Na2SO4
  5. customthe solvent was removed in vacuo
  6. customObtained brown solid
  7. filtrationthe precipitate was filtered off
  8. concentrationThe filtrate was concentrated in vacuo, and residual brown oil
  9. customwas purified by silica gel column chromatography
  10. washeluted with AcOEt and hexane (1:4-1:2)
  11. customResulting solid
  12. customwas triturated with IPE

出典と根拠

ORDレコード
ord-4f4fcff33319463ea6fc0429bb14a0a0
出典データセット
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07465731B2

反応ノート

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