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

HRID 2290539
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HRID 2290539 반응식
[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]
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참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 21867204
Cyclohexane ethylacetate
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-58e42e145d434d2d8e6eb6fa676f4d58
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04617304

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