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Phosphorus oxychloride → Ethyl 5-methyl-1,3-oxazole-2-carboxylate

HRID 2200584
ノート
印刷プレビュー

反応式

HRID 2200584 の反応式
O=[C:2]([NH:8][CH2:9][C:10](=[O:12])[CH3:11])[C:3]([O:5][CH2:6][CH3:7])=[O:4].P(Cl)(Cl)(Cl)=O>C1(C)C=CC=CC=1>[CH3:11][C:10]1[O:12][C:2]([C:3]([O:5][CH2:6][CH3:7])=[O:4])=[N:8][CH:9]=1
参加物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 24813Phosphorus oxychlorideHCID 57348900Ethyl oxo[(2-oxopropyl)amino]acetate

生成物 1

HCID 22099282Ethyl 5-methyl-1,3-oxazole-2-carboxylate収率 44.7%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a solution of ethyl 2-oxo-2-(2-oxopropylamino)acetate (1.7 g, 9.8 mmol) in toluene (10 mL) was added phosphorus oxychloride (2 mL). The mixture was heated to reflux for 3 h. The reaction was concentrated to dryness and the residue was taken up in ethyl acetate (20 mL). This organic phase was washed with saturated aqueous sodium bicarbonate solution and brine, dried and concentrated to give a crude product which was purified via silica gel chromatography eluting with petroleum ether/ethyl acetate (4:1) to give ethyl 5-methyloxazole-2-carboxylate (0.68 g, 44.1% yield) as yellow syrup. 1H-NMR (CDCl3) δ 6.97 (s, 1H), 4.44-4.49 (q, 2H), 2.43 (s, 3H), 1.42-1.46 (t, 2H). LCMS retention time 0.643 min; LCMS MH+ 156.

後処理

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 3 h
  3. concentrationThe reaction was concentrated to dryness
  4. washThis organic phase was washed with saturated aqueous sodium bicarbonate solution and brine
  5. customdried
  6. concentrationconcentrated
  7. customto give a crude product which
  8. customwas purified via silica gel chromatography
  9. washeluting with petroleum ether/ethyl acetate (4:1)

出典と根拠

ORDレコード
ord-de54447bfc9843e7848a731c4976aebc
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09359359B2

反応ノート

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