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Ethyl Propionate → 1-(4-Methyl-1,3-thiazol-2-yl)butan-2-one

HRID 1951527
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HRID 1951527 반응식
[CH3:1][C:2]1[S:3][CH:4]=[C:5]([CH3:7])[N:6]=1.C([Li])CCC.[C:13](OCC)(=[O:16])[CH2:14][CH3:15]>C1COCC1>[CH3:7][C:5]1[N:6]=[C:2]([CH2:1][C:13](=[O:16])[CH2:14][CH3:15])[S:3][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7749Ethyl PropionateHCID 109342,4-DimethylthiazoleHCID 178418339Butyllithium

생성물 1

HCID 594923371-(4-Methyl-1,3-thiazol-2-yl)butan-2-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
-78 °C

실험 절차

3.00 g (26.5 mmol) of 2,4-dimethylthiazole are dissolved in 30 ml of THF and, at −78° C., 11.6 ml (29.2 mmol) of n-butyllithium (2.5 M solution in hexane) are added dropwise. After stirring at −78° C. for 2 hours, 4.60 g (45.1 mmol) of ethyl propionate are added as solution in 15 ml of abs. THF. The mixture is stirred at −78° C. for 1 h and then warmed to room temperature. It is then hydrolyzed with sodium bicarbonate solution, and the mixture is extracted three times with diethyl ether. The combined organic phases are dried with magnesium sulfate, and the solvent is removed in a rotary evaporator. 3.5 g (39% of theory) of the title compound are obtained in 50% purity (GC-MS) and are employed without further purification.

후처리

  1. stirringThe mixture is stirred at −78° C. for 1 h
  2. temperaturewarmed to room temperature
  3. extractionhydrolyzed with sodium bicarbonate solution, and the mixture is extracted three times with diethyl ether
  4. dry with materialThe combined organic phases are dried with magnesium sulfate
  5. customthe solvent is removed in a rotary evaporator

출처 및 근거

ORD 기록
ord-05a91356a4e74a4eab01e9412d141919
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08404723B2

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