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2,6-Lutidine → 4-Formyl-2-methoxybenzonitrile

HRID 1480531
ノート
印刷プレビュー

反応式

HRID 1480531 の反応式
[CH:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]#[N:10])=[C:5]([O:11][CH3:12])[CH:4]=1)=C.N1C(C)=CC=CC=1C.I([O-])(=O)(=O)=[O:22].[Na+]>O1CCOCC1.O.[Os](=O)(=O)(=O)=O>[C:9]([C:6]1[CH:7]=[CH:8][C:3]([CH:1]=[O:22])=[CH:4][C:5]=1[O:11][CH3:12])#[N:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 79372,6-LutidineHCID 23667635Sodium periodateHCID 897251372-Methoxy-4-vinylbenzonitrile

生成物 1

HCID 600485344-Formyl-2-methoxybenzonitrile

試薬・触媒・溶媒 3

HCID 30318Osmium Tetroxide触媒HCID 962Water溶媒2 回
HCID 31275
1,4-Dioxane
溶媒

実験手順

To a solution of 1-vinyl-4-cyano-3-methoxybenzene (0.343 g, 2.16 mmol, 1.0 eq) in dioxane (7 mL) was added 2,6-lutidine (0.461 g, 0.50 mL, 4.31 mmol, 2.0 eq) followed by osmium tetroxide (1.37 g, 1.32 mL of a 4% solution in water, 0.22 mmol, 0.1 eq). A brown/black solution resulted after 1→2 minutes. Sodium periodate (1.847 g, 8.63 mmol as a solution in 7 mL of water, 4.0 eq) was added forming a white precipitate. The mixture was stirred at room temperature for 35 minutes before partitioning between EtOAc (100 mL) and HCl (1M, 100 mL). The organics were washed with brine (100 mL), dried (Na2SO4) and concentrated under reduced pressure. MPLC (10→50% EtOAc-hexane) yielded the title compound as a white solid; 1H nmr (CDCl3) d 9.89 (1H, s, CHO), 8.09 (2H, m, ArH-2, H-6), 7.12 (1H, d, J 9.5 Hz, ArH-3), 4.04 (3H, s, OCH3); m/z 162 [M+H]+.

後処理

  1. customA brown/black solution resulted after 1→2 minutes
  2. customforming a white precipitate
  3. custombefore partitioning between EtOAc (100 mL) and HCl (1M, 100 mL)
  4. washThe organics were washed with brine (100 mL)
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-a98e4f3c9b5c4b819de8d652cd3cc29e
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409884B2

反応ノート

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