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

HRID 544965
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HRID 544965 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]
참가 물질실험 절차후처리출처 및 근거반응 노트

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)).

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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-bfe285ab1c6e4fd0adfd2d68fd8d7ec5
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07935704B2

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