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1-Iodopropane → HCID 44549790, 화합물

HRID 2377061
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HRID 2377061 반응식
[Na].[CH3:2][C:3]1[NH:4][O:5][C:6](=[O:13])[C:7]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9].I[CH2:15][CH2:16][CH3:17]>CN(C=O)C>[CH3:2][C:3]1[N:4]([CH2:15][CH2:16][CH3:17])[O:5][C:6](=[O:13])[C:7]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9]
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참가 물질

4

반응물 2

HCID 336431-IodopropaneHCID 69198820HCID 69198820, 화합물

생성물 1

HCID 44549790HCID 44549790, 화합물수율 13.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
120 °C

실험 절차

To a stirred solution of ethyl 3-methyl-5-oxo-2,5-dihydroisoxazole-4-carboxylate sodium salt [prepared according G. Doleschall, Tetrahedron Lett. 1987, 28, 2993-2994] (3.5 g, 18.1 mmol) in DMF (20 mL) was added 1-iodopropane (1.70 g, 18.1 mmol). The resulting mixture was heated to 120° C. for 1 hr. When cooled down, it was poured into ice-water (30 mL), and extracted with dichloromethane (2×50 mL). The organic layer was washed with water (2×50 mL), dried over sodium sulfate, concentrated and purified by flash chromatography with ethyl acetate/hexanes (1/1) to provide a solid product (0.52 g, 13% yield). 1H NMR (CDCl3) δ ppm 4.33 (q, 2H, J=7.1 Hz), 3.86 (t, 2H, J=6.8 Hz), 2.57 (s, 3H), 1.81-1.88 (m, 2H), 1.37 (t, 3H, J=7.1 Hz), 0.98 (t, 3H, J=7.6 Hz). LCMS (APCI, M+H+): 214.1.

후처리

  1. temperatureWhen cooled down
  2. extractionextracted with dichloromethane (2×50 mL)
  3. washThe organic layer was washed with water (2×50 mL)
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. custompurified by flash chromatography with ethyl acetate/hexanes (1/1)

출처 및 근거

ORD 기록
ord-f41cdd2c417a4070b9240f44e52d250f
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07468375B2

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