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Sodium Carbonate → 1,2-Epoxy-3,4-(dimethylmethylenedioxy)-5-hexene

HRID 1741950
ノート
印刷プレビュー

反応式

HRID 1741950 の反応式
C1(C)C=CC(S(O[CH2:11][CH:12]([OH:22])[CH:13]2[O:19][C:18]([CH3:21])([CH3:20])[O:17][CH:14]2[CH:15]=[CH2:16])(=O)=O)=CC=1.C(=O)([O-])[O-].[Na+].[Na+]>CO>[O:22]1[CH:12]([CH:13]2[O:19][C:18]([CH3:20])([CH3:21])[O:17][CH:14]2[CH:15]=[CH2:16])[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

4

反応物 2

HCID 10340Sodium CarbonateHCID 190109853,4-(Dimethylmethylenedioxy)-2-hydroxy-5-hexen-1-yl p-toluenesulfonate

生成物 1

HCID 100123231,2-Epoxy-3,4-(dimethylmethylenedioxy)-5-hexene収率 88.5%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

3,4-(Dimethylmethylenedioxy)-2-hydroxy-5-hexen-1-yl p-toluenesulfonate (17.88 g) was dissolved in ml of methanol, and 17.11 g of anhydrous sodium carbonate was added at room temperature, followed by stirring the mixture for 15 minutes. The reaction mixture was filtered through Celite, and crystals were washed with diethyl ether. After the filtrate was concentrated, the solid was filtered through a silica gel column. The filtrate was concentrated under reduced pressure to obtain 7.87 g of 1,2-epoxy-3,4-(dimethylmethylenedioxy)-5-hexene having the following properties.

後処理

  1. additionwas added at room temperature
  2. filtrationThe reaction mixture was filtered through Celite, and crystals
  3. washwere washed with diethyl ether
  4. concentrationAfter the filtrate was concentrated
  5. filtrationthe solid was filtered through a silica gel column
  6. concentrationThe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-f33abe414fcb46f6954500ae52f20fcb
出典データセット
uspto-grants-1994_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05334740

反応ノート

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