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Pyridine → Ethyl 4-(methoxycarbonylmethoxy)acetoacetate

HRID 462462
ノート
印刷プレビュー

反応式

HRID 462462 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 13457217Ethyl 4-(methoxycarbonylmethoxy)acetoacetate収率 12.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
5 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-96d5dc5cd7ea4545b5178e560b4f64b5
出典データセット
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04515799

反応ノート

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