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Water → (2-Ethenylcyclopropane-1,1-diyl)dimethanol

HRID 2290539
ノート
印刷プレビュー

反応式

HRID 2290539 の反応式
[CH:1]([CH:3]1[CH2:5][C:4]1([C:11](OCC)=[O:12])[C:6](OCC)=[O:7])=[CH2:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].O>O1CCCC1.C1CCCCC1.C(OCC)(=O)C>[OH:7][CH2:6][C:4]1([CH2:11][OH:12])[CH2:5][CH:3]1[CH:1]=[CH2:2]
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 3

HCID 962WaterHCID 111025Diethyl 2-vinylcyclopropane-1,1-dicarboxylateHCID 21226445Aluminium lithium hydride

生成物 1

HCID 13572991(2-Ethenylcyclopropane-1,1-diyl)dimethanol収率 93.2%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 21867204
Cyclohexane ethylacetate
溶媒

実験手順

A solution of 23 g (0.108 mole) of diethyl 2-vinylcyclopropane-1,1-dicarboxylate in 90 ml of dry THF (tetrahydrofuran) was added dropwise to 196 ml of 1M LAH (lithium aluminum hydride) which was stirred and heated at 68°. The addition required 30 minutes and heating and stirring were continued for 2 hours. TLC in cyclohexane-ethyl acetate (1:1) and CHCl3MeOH (9:1) showed that the reaction was complete. The reaction was cooled to 0° and a total of 200 ml of water was continuously added. After being stirred for 15 minutes, the mixture was filtered and the solid was washed with THF. The combined filtrates were concentrated to yield 12.9 g (93%) of the title compound, RfCHCl3 -MeOH (9:1) 0.45.

後処理

  1. temperatureheated at 68°
  2. additionThe addition required 30 minutes
  3. temperatureheating
  4. stirringstirring
  5. temperatureThe reaction was cooled to 0°
  6. stirringAfter being stirred for 15 minutes
  7. filtrationthe mixture was filtered
  8. washthe solid was washed with THF
  9. concentrationThe combined filtrates were concentrated

出典と根拠

ORDレコード
ord-58e42e145d434d2d8e6eb6fa676f4d58
出典データセット
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04617304

反応ノート

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