Acetone → Ethyl 2-[2-(4-bromophenyl)-2-oxoethyl]pentanoate

HRID 907664노트

반응식

HRID 907664 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:20])[CH2:9][C:10]([CH2:17][CH2:18][CH3:19])([C:14]([O-:16])=[O:15])C([O-])=O)=[CH:4][CH:3]=1.[CH3:21][C:22](C)=O.[OH-].[Na+]>C(O)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8](=[O:20])[CH2:9][CH:10]([CH2:17][CH2:18][CH3:19])[C:14]([O:16][CH2:21][CH3:22])=[O:15])=[CH:6][CH:7]=1

참가 물질

5

반응물 3

HCID 180AcetoneHCID 14798Sodium HydroxideHCID 219858152-[2-(4-Bromophenyl)-2-oxoethyl]-2-propylmalonate

생성물 1

HCID 21985789Ethyl 2-[2-(4-bromophenyl)-2-oxoethyl]pentanoate수율 20%

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
55 °C

실험 절차

To a 200 mL flask was added crude 2-[2-(4-bromophenyl)-2-oxoethyl]-2-propylmalonate (7.62 g, 19.2 mmol), acetone (21 mL), and ethanol (19 mL), followed by addition of 1 N aqueous sodium hydroxide solution (19.1 mL). The reaction mixture was heated to 55° C. for 3 h. The clear, orange-red reaction mixture was then concentrated under reduced pressure and the residue was redissolved in dimethoxyethane (30 mL). The mixture was heated to 80° C. for 3 h. The reaction mixture was cooled to rt, diluted with ethyl acetate (100 mL) and water (100 mL), and stirred for 15 minutes until almost all color was extracted into the organic layer. The layers were separated and the aqueous layer extracted with additional ethyl acetate (75 mL). The combined organic layers were washed with saturated aqueous sodium chloride solution (75 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford an orange oil. The crude product was purified by flash chromatography (10:1 hexane:ethyl acetate) to afford ethyl 2-[2-(4-bromophenyl)-2-oxoethyl]pentanoate (1.33 g, 20%). LC-MS ret. time 3.60 min, m/z 326.05 (MH+); 1H NMR (300 MHz, CDCl3) δ 0.87 (t, 3H), 1.25 (t, 3H), 1.29-1.43 (m, 2H), 1.57-1.73 (m, 2H), 2.90-3.08 (m, 2H), 3.34-3.47 (m, 2H), 4.15 (q, 21), 7.59 (d, 4), 7.82 (d, 2H).

후처리

  1. concentrationThe clear, orange-red reaction mixture was then concentrated under reduced pressure
  2. dissolutionthe residue was redissolved in dimethoxyethane (30 mL)
  3. temperatureThe mixture was heated to 80° C. for 3 h
  4. temperatureThe reaction mixture was cooled to rt
  5. additiondiluted with ethyl acetate (100 mL) and water (100 mL)
  6. extractionwas extracted into the organic layer
  7. customThe layers were separated
  8. extractionthe aqueous layer extracted with additional ethyl acetate (75 mL)
  9. washThe combined organic layers were washed with saturated aqueous sodium chloride solution (75 mL)
  10. dry with materialdried over anhydrous sodium sulfate
  11. concentrationconcentrated under reduced pressure
  12. customto afford an orange oil
  13. customThe crude product was purified by flash chromatography (10:1 hexane:ethyl acetate)

출처 및 근거

ORD 기록
ord-0d3dbb643ea64b28a229689b82161f23
출처 데이터셋
uspto-grants-2011_09
특허 번호
US08013166B2

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