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Ethyl 2,4-dioxovalerate → 4-Acetyl-3-hydroxy-1H-pyrrol-2(5H)-one

HRID 234724
ノート
印刷プレビュー

反応式

HRID 234724 の反応式
[O:1]=[C:2]([CH2:8][C:9](=[O:11])[CH3:10])[C:3]([O:5]CC)=O.[Cl-].C[C:14](=[NH2+:16])C>C(#N)C>[C:9]([C:8]1[CH2:14][NH:16][C:3](=[O:5])[C:2]=1[OH:1])(=[O:11])[CH3:10]
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

4

反応物 2

HCID 69208Ethyl 2,4-dioxovalerateHCID 21939857Dimethylmethyleneammonium chloride

生成物 1

HCID 233554434-Acetyl-3-hydroxy-1H-pyrrol-2(5H)-one収率 33.9%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
-40 °C

実験手順

A solution of ethyl 2,4-dioxovalerate (1.13 g, 7.11 mmole), dimethylmethylene ammonium chloride (0.67 g, 7.11 mmole) and acetonitrile (3 ml) was stirred at 25° C. over 45 minutes. The resulting yellow homogeneous solution was then cooled to -40° C. and ammonia gas was bubbled through the mixture over 5 minutes, during which time a yellow solid precipitated out of solution. The stirred mixture was allowed to slowly warm to 5° C. over a period of 1 hour before addition of concentrated ammonium hydroxide (4 ml). After stirring for 1 hour, the mixture was concentrated under reduced pressure, diluted with 3N HCl (6 ml) and extracted with ethyl acetate (50 ml×10). The combined organics were dried over sodium sulfate, filtered and concentrated under reduced pressure to give 0.34 g of the title compound as a yellow amorphous solid. M.P. 178°-180° C. (dec); 1H nmr (250 MHz, DMSO-d6) δ2.42 (s, 3H), 3.78 (s, 2H), 8.87 (s, 1H); Anal. calcd. for C6H7NO3 : C, 51.07; H, 5.00; N, 9.92. Found: C, 51.18; H, 5.23; N, 9.73.

後処理

  1. customammonia gas was bubbled through the mixture over 5 minutes, during which time a yellow solid
  2. customprecipitated out of solution
  3. temperatureto slowly warm to 5° C. over a period of 1 hour before addition of concentrated ammonium hydroxide (4 ml)
  4. concentrationthe mixture was concentrated under reduced pressure
  5. additiondiluted with 3N HCl (6 ml)
  6. extractionextracted with ethyl acetate (50 ml×10)
  7. dry with materialThe combined organics were dried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-08f430d91fcc4836ba383269365fd0ff
出典データセット
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05596013

反応ノート

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