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1,2-Dichloroethane → 1,3,3-Trimethyl-2-oxabicyclo(2.2.2)octan-6-one

HRID 426576
ノート
印刷プレビュー

反応式

HRID 426576 の反応式
[CH3:1][C:2]1[CH2:7][CH2:6][C@H:5]([C:8]([OH:11])([CH3:10])[CH3:9])[CH2:4][CH:3]=1.ClC1C=CC=C(C(OO)=[O:20])C=1.C(Cl)CCl.[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1>C(Cl)Cl>[CH3:1][C:2]12[CH2:7][CH2:6][CH:5]([CH2:4][C:3]1=[O:20])[C:8]([CH3:10])([CH3:9])[O:11]2
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 4

HCID 111,2-DichloroethaneHCID 70297m-Chloroperbenzoic acidHCID 443162(L)-alpha-terpineolHCID 178418287HCID 178418287、化合物

生成物 1

HCID 1122031,3,3-Trimethyl-2-oxabicyclo(2.2.2)octan-6-one

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A mixture of 3.08 g. (0.02 mole) α-terpineol and 4.45 g. (0.022 mole) of 85 percent m-chloroperbenzoic acid in 70 ml. of ethylene dichloride is refluxed under nitrogen for 20 hours, then cooled to room temperature and washed with aqueous sodium bisulfite and sodium bicarbonate solutions. The solvent is removed in vacuo and the resulting oil is treated in situ with 2.94 g. (0.0136 mole) pyridinium chlorochromate. The resulting mixture is stirred under nitrogen in 35 ml. of methylene chloride at ambient temperatures for 2.5 hours. After addition of 200 ml. diethyl ether, the mixture is filtered through celite and the solvent evaporated to give, on steam distillation, 1,3,3-trimethyl-2-oxabicyclo [2,2,2]octan-6-one; m.p. 50° to 52° C.

後処理

  1. additionA mixture of 3.08 g
  2. washwashed with aqueous sodium bisulfite and sodium bicarbonate solutions
  3. customThe solvent is removed in vacuo
  4. additionthe resulting oil is treated in situ with 2.94 g
  5. additionAfter addition of 200 ml
  6. filtrationdiethyl ether, the mixture is filtered through celite
  7. customthe solvent evaporated

出典と根拠

ORDレコード
ord-f5359b997e454ac181e33e29059008cf
出典データセット
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04170599

反応ノート

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