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Ethyl Acetate → (RS)-5-methoxymethyl-3-pyridin-3-yl-oxazolidin-2-one

HRID 1900080
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HRID 1900080 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([NH:7]C(=O)OCC)[CH:2]=1.[CH3:13][O:14][CH2:15][CH:16]1[CH2:20][O:19][C:18](=O)[O:17]1.C(=O)([O-])[O-].[K+].[K+].C(OCC)(=O)C>O>[CH3:13][O:14][CH2:15][CH:16]1[O:17][C:18](=[O:19])[N:7]([C:3]2[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=2)[CH2:20]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 235275ethyl N-(pyridin-3-yl)carbamateHCID 43844854-(Methoxymethyl)-1,3-dioxolan-2-one

생성물 1

HCID 23371844(RS)-5-methoxymethyl-3-pyridin-3-yl-oxazolidin-2-one수율 83.6%

시약·촉매·용매 1

HCID 962
Water
용매

실험 절차

A mixture of 16.8 g of ethyl pyridin-3-yl-carbamate, 20 g of 4-methoxymethyl-1,3-dioxolan-2-one and 2.8 g of potassium carbonate was heated to 160° for 3 h. The mixture was cooled and treated with ethyl acetate and water. The phases were separated, the aqueous phase was extracted with ethyl acetate and the organic phase was washed with saturated sodium chloride solution. The organic phases were combined, dried with magnesium sulfate and concentrated. Chromatography of the residue (21 g) on silica gel with ethyl acetate/methanol mixtures (1:0-20:1) yielded 17.6 g of (RS)-5-methoxymethyl-3-pyridin-3-yl-oxazolidin-2-one which was recrystallized from diethyl ether. M.p.: 65°-66°.

후처리

  1. temperaturewas heated to 160° for 3 h
  2. temperatureThe mixture was cooled
  3. customThe phases were separated
  4. extractionthe aqueous phase was extracted with ethyl acetate
  5. washthe organic phase was washed with saturated sodium chloride solution
  6. dry with materialdried with magnesium sulfate
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-d73a93bad73545f995fbe6d612e2a198
출처 데이터셋
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05574055

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