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Sodium periodate → 6,7-Dihydro-[1,4]dioxino[2,3-c]pyridazine-3-carbaldehyde

HRID 1943255
ノート
印刷プレビュー

反応式

HRID 1943255 の反応式
[CH:1]([C:3]1[N:8]=[N:7][C:6]2[O:9][CH2:10][CH2:11][O:12][C:5]=2[CH:4]=1)=C.I([O-])(=O)(=O)=[O:14].[Na+]>O1CCOCC1.O.[Os](=O)(=O)(=O)=O>[N:7]1[C:6]2[O:9][CH2:10][CH2:11][O:12][C:5]=2[CH:4]=[C:3]([CH:1]=[O:14])[N:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 23667635Sodium periodateHCID 675264353-Vinyl-6,7-dihydro-[1,4]dioxino[2,3-c]pyridazine

生成物 1

HCID 248916966,7-Dihydro-[1,4]dioxino[2,3-c]pyridazine-3-carbaldehyde収率 64.4%

試薬・触媒・溶媒 2

HCID 30318Osmium Tetroxide触媒HCID 218864351,4-Dioxane--water (1/1)溶媒

実験手順

A solution of 3-ethenyl-6,7-dihydro[1,4]dioxino[2,3-c]pyridazine (11.58 g) in 1,4-dioxane/water (600 ml/180 ml), cooled in ice, was treated with an aqueous solution of osmium tetroxide (4% w/v, 25 ml) and sodium periodate (43 g). This mixture was allowed to warm to room temperature and after 7 hours under stirring the mixture was evaporated to dryness and azeotroped with 1,4-dioxane. Silica gel, 1,4-dioxane and chloroform were added and the mixture was evaporated to dryness overnight, then added to a silica column (400 g) and chromatographed, eluting with chloroform then 0-100% ethyl acetate in hexane, to afford a white solid (7.55 g, 64%).

後処理

  1. customwas evaporated to dryness
  2. customazeotroped with 1,4-dioxane
  3. additionSilica gel, 1,4-dioxane and chloroform were added
  4. customthe mixture was evaporated to dryness overnight
  5. additionadded to a silica column (400 g)
  6. customchromatographed
  7. washeluting with chloroform

出典と根拠

ORDレコード
ord-fcd3b323248f459290826226c0b4b494
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08389524B2

反応ノート

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