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Pyridine → Ethyl 4-(methoxycarbonylmethoxy)acetoacetate

HRID 462462
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HRID 462462 반응식
Cl[C:2]([CH2:4][O:5][CH2:6][C:7]([O:9][CH3:10])=[O:8])=[O:3].[CH3:11][C:12]1(C)[O:17]C(=O)[CH2:15][C:14](=O)[O:13]1.N1C=CC=CC=1>ClCCl>[CH3:10][O:9][C:7]([CH2:6][O:5][CH2:4][C:2](=[O:3])[CH2:11][C:12]([O:13][CH2:14][CH3:15])=[O:17])=[O:8]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 162492,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 12361282Methyl (2-chloro-2-oxoethoxy)acetate

생성물 1

HCID 13457217Ethyl 4-(methoxycarbonylmethoxy)acetoacetate수율 12.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
5 °C

실험 절차

Methyl 2-(chloroformylmethoxy)acetate (216.6 g) was added over 45 minutes to a stirred solution of 2,2-dimethyl-1,3-dioxane-4,6-dione (173.9 g) and pyridine (189.6 g) in dichloromethane (1000 ml) keeping the temperature below 5° C. The mixture was stirred at 5° C. for 30 minutes, allowed to warm up to room temperature over one hour, washed with 2.4M hydrochloric acid and water, dried over magnesium sulphate and evaporated. The resulting brown oil was dissolved in ethanol (300 ml) and the solution heated under reflux for 2.5 hours and evaporated. The residual oil was distilled to give the title compound (32.5 g), b.p. 138°-140°/1 torr which was characterised by its N.m.r. spectrum in CDCl3, δ values: 4.27 (2H,s); 4.20 (2H, q, J 7 Hz); 4.16 (2H,s); 3.75 (3H, s); 3.54 (2H, s); 1.29 (3H, t, J 7 Hz).

후처리

  1. customthe temperature below 5° C
  2. temperatureto warm up to room temperature over one hour
  3. washwashed with 2.4M hydrochloric acid and water
  4. dry with materialdried over magnesium sulphate
  5. customevaporated
  6. dissolutionThe resulting brown oil was dissolved in ethanol (300 ml)
  7. temperaturethe solution heated
  8. temperatureunder reflux for 2.5 hours
  9. customevaporated
  10. distillationThe residual oil was distilled

출처 및 근거

ORD 기록
ord-96d5dc5cd7ea4545b5178e560b4f64b5
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04515799

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