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Pyridine → Ethyl 4-(methoxycarbonylmethoxy)acetoacetate

HRID 2290327
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HRID 2290327 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, allowing 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 browm 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°/l 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 browm 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-9a830c34682e4d26bc6c765c40153146
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04616024

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