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Phosphorus oxide (P4O10) → Methyl 5-methoxy-1,3-oxazole-2-carboxylate

HRID 1817293
ノート
印刷プレビュー

反応式

HRID 1817293 の反応式
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[CH3:15][O:16][C:17](=[O:26])[C:18]([NH:20][CH2:21][C:22]([O:24][CH3:25])=O)=[O:19]>C(#N)C>[CH3:25][O:24][C:22]1[O:19][C:18]([C:17]([O:16][CH3:15])=[O:26])=[N:20][CH:21]=1
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 14812Phosphorus oxide (P4O10)HCID 560326Dimethyloxalylglycine

生成物 1

HCID 1491126Methyl 5-methoxy-1,3-oxazole-2-carboxylate

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
65 °C

実験手順

To a warm (35-40° C.) suspension of phosphorous pentoxide (77.7 g, 109 mmol) in anhydrous acetonitrile (200 mL) was added methyl[(2-methoxy-2-oxoethyl)amino](oxo)acetate (19.19 g, 109.6 mmol). The reaction mixture was heated to 65° C., then stirred overnight at room temperature. The product mixture was cooled to 0° C. and carefully quenched with ice and brine keeping the reaction from generating an unsuitable exotherm. The resultant mixture was extracted with ethyl acetate (600 mL). The organic extract was washed with brine, dried with Na2SO4, then concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 100% CH2Cl2. The appropriate fractions were combined and concentrated to afford the title compound as a light yellow solid that was used without further purification.

後処理

  1. temperatureTo a warm
  2. temperatureThe product mixture was cooled to 0° C.
  3. customcarefully quenched with ice and brine keeping
  4. customthe reaction
  5. extractionThe resultant mixture was extracted with ethyl acetate (600 mL)
  6. extractionThe organic extract
  7. washwas washed with brine
  8. dry with materialdried with Na2SO4
  9. concentrationconcentrated under vacuum
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-73364039a1844d138608c16198ebf673
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07598264B2

反応ノート

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