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Sodium periodate → 2-Oxo-1-(2-oxoethyl)-1,2-dihydroquinoline-7-carbonitrile

HRID 656891
ノート
印刷プレビュー

反応式

HRID 656891 の反応式
[O:1]=[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][C:6]([C:12]#[N:13])=[CH:7][CH:8]=2)[N:3]1[CH2:14][CH:15]=C.I([O-])(=O)(=O)=[O:18].[Na+]>O1CCOCC1.O.O=[Os](=O)(=O)=O>[O:1]=[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][C:6]([C:12]#[N:13])=[CH:7][CH:8]=2)[N:3]1[CH2:14][CH:15]=[O:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 23667635Sodium periodate2 回HCID 689923622-Oxo-1-(2-propen-1-yl)-1,2-dihydro-7-quinolinecarbonitrile

生成物 1

HCID 602002792-Oxo-1-(2-oxoethyl)-1,2-dihydroquinoline-7-carbonitrile収率 107.2%

試薬・触媒・溶媒 3

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

実験手順

A solution of 2-oxo-1-(2-propen-1-yl)-1,2-dihydro-7-quinolinecarbonitrile (600 mg, 2.9 mmol) in 1,4-dioxane (30 ml) and water (20 ml) was cooled to 0° C. and treated with OsO4 (4% in water, 3 ml) and sodium periodate (1.4 g, 6.67 mmol). The reaction was warmed to rt; 0.6 g and then 3.7 g more of sodium periodate were added. After 4 h in total, the solvent was evaporated and residue partitioned between water and 20% methanol-DCM. The phases were separated and the organic phase was dried and evaporated to afford the desired compound (660 mg, 107%).

後処理

  1. customthe solvent was evaporated
  2. customresidue partitioned between water and 20% methanol-DCM
  3. customThe phases were separated
  4. customthe organic phase was dried
  5. customevaporated

出典と根拠

ORDレコード
ord-d19ed902b1004bd3ba55bea1477e54d6
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08071592B2

反応ノート

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