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Hydrochloric Acid → Methyl 3-(i-propylsulfonyl)-2-oxopropanoate

HRID 2037192
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HRID 2037192 반응식
[CH:1]([S:4]([CH3:7])(=[O:6])=[O:5])([CH3:3])[CH3:2].CO.C[O-].[Na+].[C:13]([O:18][CH3:19])(=[O:17])[C:14]([O-])=[O:15].Cl>C1COCC1>[CH:1]([S:4]([CH2:7][C:14](=[O:15])[C:13]([O:18][CH3:19])=[O:17])(=[O:6])=[O:5])([CH3:3])[CH3:2]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 1383722-(Methylsulphonyl)propaneHCID 21923985Methoxy(oxo)acetateHCID 23694274Sodium methanolate methanol

생성물 1

HCID 58365407Methyl 3-(i-propylsulfonyl)-2-oxopropanoate수율 30.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

실험 절차

To a mixture of i-propylmethylsulfone (5.17 g, 42.3 mmol) and THF (20 mL) was added 28% sodium methoxide methanol solution (8.58 g, 44.5 mmol) at room temperature, and then methyl oxalate (5.0 g, 42.3 mmol) was gradually added to the mixture at room temperature. The resulting mixture was stirred at room temperature overnight. To the reaction mixture was added ice-water (200 mL), and the pH of the resulting mixture was adjusted pH3 or less than pH3 with 2 mol/L hydrochloric acid. The mixture was extracted with ethyl acetate (200 mL). The extract was washed with brine (200 mL), dried over anhydrous sodium sulphate, and concentrated in vacuo. The resulting residue was purified on a silica gel column chromatography (ethyl acetate/n-hexane) to give methyl 3-(i-propylsulfonyl)-2-oxopropanoate (2.7 g, yield: 28%) as colorless oil.

후처리

  1. extractionThe mixture was extracted with ethyl acetate (200 mL)
  2. washThe extract was washed with brine (200 mL)
  3. dry with materialdried over anhydrous sodium sulphate
  4. concentrationconcentrated in vacuo
  5. customThe resulting residue was purified on a silica gel column chromatography (ethyl acetate/n-hexane)

출처 및 근거

ORD 기록
ord-a56f7a0bba914725ac3a5fcbdc7a287f
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08575197B2

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