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2,2-Dimethyl-3-(toluene-4-sulfonyloxy)butyric acid methyl ester → 2,2-Dimethyl-3-butenoic acid methyl ester

HRID 1092733
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HRID 1092733 반응식
[CH3:1][O:2][C:3](=[O:20])[C:4]([CH3:19])([CH3:18])[CH:5](OS(C1C=CC(C)=CC=1)(=O)=O)[CH3:6]>C1CCN2C(=NCCC2)CC1.CCOCC>[CH3:1][O:2][C:3](=[O:20])[C:4]([CH3:19])([CH3:18])[CH:5]=[CH2:6]
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참가 물질

4

반응물 1

HCID 210314932,2-Dimethyl-3-(toluene-4-sulfonyloxy)butyric acid methyl ester

생성물 1

HCID 116939102,2-Dimethyl-3-butenoic acid methyl ester수율 130%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene용매

실험 절차

A solution of 2,2-dimethyl-3-(toluene-4-sulfonyloxy)-butyric acid methyl ester (18.06 g, 0.06 mol) in DBU (15 ml) was heated at 140-160° for 3.5 h. The mixture was allowed to cool to room temperature and was then diluted with ether. The mixture was washed with HCl (1 M), sodium bicarbonate, then brine. The ethereal layer was dried and partially evaporated to give a concentrated solution of 2,2-dimethyl-but-3-enoic acid methyl ester (10 g). (Savu and Katzenellenbogen, J. Org. Chem, 46:239-250 (1981)). Further evaporation was avoided due to the volatility of the product (bp 102°). (Tsaconas et al., Aust. J. Chem., 53:435-437 (2000)).

후처리

  1. washThe mixture was washed with HCl (1 M), sodium bicarbonate
  2. customThe ethereal layer was dried
  3. custompartially evaporated

출처 및 근거

ORD 기록
ord-6324124b2147447ab24fb4b80c5e9abe
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08129527B2

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