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1,4-Dioxane → 1-(Methoxymethyl)-3-oxocyclobutane-1-carbonitrile

HRID 1692921
ノート
印刷プレビュー

反応式

HRID 1692921 の反応式
[O:1]1CCOCC1.[CH3:7][O:8][CH2:9][C:10]1([C:15]#[N:16])[CH2:13][C:12](=C)[CH2:11]1.I([O-])(=O)(=O)=O.[Na+]>O.[Os](=O)(=O)(=O)=O>[CH3:7][O:8][CH2:9][C:10]1([C:15]#[N:16])[CH2:13][C:12](=[O:1])[CH2:11]1
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 3

HCID 312751,4-DioxaneHCID 23667635Sodium periodateHCID 668243071-(Methoxymethyl)-3-methylidenecyclobutane-1-carbonitrile

生成物 1

HCID 668243301-(Methoxymethyl)-3-oxocyclobutane-1-carbonitrile

試薬・触媒・溶媒 2

HCID 30318Osmium Tetroxide触媒HCID 962Water溶媒2 回

実験手順

A mixture of water (2 mL, 0.1 mol) and 1,4-dioxane (7 mL, 0.08 mol), 1-(methoxymethyl)-3-methylenecyclobutanecarbonitrile (0.294 g, 0.00214 mol), and 0.2 M of osmium tetraoxide in water (0.04 mL) was stirred for 5 min, during which time the mixture became brown. While the temperature was maintained at room temperature, sodium periodate (0.963 g, 0.00450 mol) was added in portions over a period of 30 min. The mixture was stirred overnight. The mixture was extracted with EtOAc and the combined organic layers were dried over MgSO4. After removal of the solvents, the crude product was used directly in next step (298 mg, 99.92%). 1H NMR (400 MHz, CDCl3): 3.70 (2H, s), 3.68 (3H, s), 3.58 (2H, m), 3.38 (2H, m) ppm.

後処理

  1. stirringThe mixture was stirred overnight
  2. extractionThe mixture was extracted with EtOAc
  3. dry with materialthe combined organic layers were dried over MgSO4
  4. customAfter removal of the solvents

出典と根拠

ORDレコード
ord-8ea74a97d5ac4d97a808eaf3bc540c3b
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08158616B2

反応ノート

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