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Diethyl Ether → [(3-Methylidenecyclobutoxy)methyl]benzene

HRID 1966838
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HRID 1966838 반응식
[I-].[Na+].N12CCCN=C1CCCCC2.CS(O[CH2:19][CH:20]1[CH2:23][CH:22]([O:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH2:21]1)(=O)=O.C(OCC)C>C(COC)OC.O>[CH2:19]=[C:20]1[CH2:23][CH:22]([O:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH2:21]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 3283Diethyl EtherHCID 5238Sodium IodideHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 86647603(3-(Benzyloxy)cyclobutyl)methyl methanesulfonate

생성물 1

HCID 66732815[(3-Methylidenecyclobutoxy)methyl]benzene

시약·촉매·용매 2

HCID 962Water용매
HCID 8071
1,2-Dimethoxyethane
용매

실험 절차

Sodium iodide (0.45 gm, 3 mmol) and 1,8-diazabicyclo (5.4.0)undec-7-ene (0.304 gm, 2 mmol) were added to a stirred solution of [3-(benzyloxy)cyclobutyl]methyl methanesulfonate (0.27 gm, 1 mmol) (step b) in dimethoxyethane and the reaction mixture was refluxed for about 2 hours. It was allowed to come to room temperature and then was stirred with diethyl ether and water for about 10 minutes. The ether layer was separated and aqueous layer was washed with ether. The combined organic layer was washed with brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude compound was purified over silica gel.

후처리

  1. temperaturethe reaction mixture was refluxed for about 2 hours
  2. customto come to room temperature
  3. customThe ether layer was separated
  4. washaqueous layer was washed with ether
  5. washThe combined organic layer was washed with brine
  6. dry with materialdried over anhydrous sodium sulphate
  7. concentrationconcentrated under reduced pressure
  8. customThe crude compound was purified over silica gel

출처 및 근거

ORD 기록
ord-b45a397891784fa3a91d9374d76d5f5d
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08420666B2

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