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Ethyl Acrylate → HCID 68105235、化合物

HRID 1026550
ノート
印刷プレビュー

反応式

HRID 1026550 の反応式
Cl[C:2]1[C:7]([NH2:8])=[CH:6][C:5]([Cl:9])=[CH:4][N:3]=1.C1(P(C2C=CC=CC=2)CCCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:40]([O:44][CH2:45][CH3:46])(=[O:43])[CH:41]=[CH2:42].C(N(C(C)C)CC)(C)C>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O.C(OCC)(=O)C.CN(C)C=O>[NH2:8][C:7]1[C:2](/[CH:42]=[CH:41]/[C:40]([O:44][CH2:45][CH3:46])=[O:43])=[N:3][CH:4]=[C:5]([Cl:9])[CH:6]=1
参加物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 81531DiisopropylethylamineHCID 821241,4-Bis(diphenylphosphino)butaneHCID 27999993-Amino-2,5-dichloropyridine

生成物 1

HCID 68105235HCID 68105235、化合物

試薬・触媒・溶媒 5

HCID 74236Tetrabutylammonium Bromide触媒
HCID 167845
palladium(II) acetate
触媒
HCID 962Water溶媒
HCID 6228Dimethylformamide溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

A N,N-dimethylformamide suspension (406 ml) of 2,5-dichloropyridine-3-amine (81.2 g), palladium acetate (11.2 g), 1,4-bis(diphenylphosphino)butane (42.5 g), ethyl acrylate (109 ml), diisopropylethylamine (174 ml) and tetrabutylammonium bromide (161 g) was stirred at 140° C. for 30 hours. After the reaction solution was brought back to room temperature, ethyl acetate and water were added and the solution was separated, and the aqueous layer was extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. To the residue was added a 50% ethyl acetate-hexane mixed solvent, followed by stirring. The insolubles were filtered off, and washed with ethyl acetate, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to afford ethyl (2E)-3-(3-amino-5-chloropyridin-2-yl)acrylate (50.6 g).

後処理

  1. customwas brought back to room temperature
  2. customthe solution was separated
  3. extractionthe aqueous layer was extracted with ethyl acetate
  4. dry with materialThe combined organic layer was dried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. additionTo the residue was added a 50% ethyl acetate-hexane mixed solvent
  7. filtrationThe insolubles were filtered off
  8. washwashed with ethyl acetate
  9. concentrationthe filtrate was concentrated under reduced pressure
  10. customThe residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-9d5f5b49df52407db5e4bca0320c6087
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08729095B2

反応ノート

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