1,3-Dichloroacetone → 4-(Chloromethyl)-2-pentyloxazole

HRID 1608665

反応式

HRID 1608665 の反応式
[C:1]([NH2:8])(=[O:7])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[Cl:9][CH2:10][C:11]([CH2:13]Cl)=O.[OH-].[Na+]>OS(O)(=O)=O>[CH2:2]([C:1]1[O:7][CH:13]=[C:11]([CH2:10][Cl:9])[N:8]=1)[CH2:3][CH2:4][CH2:5][CH3:6]

参加物

5

反応条件

温度
120 °C

実験手順

The synthesis of 3 was performed similarly to example 1 above. The solids, hexanoamide (5 g) and 1,3-dichloroacetone (5.5 g), were mixed together in a round bottomed flask and heated at 120° C. under an argon atmosphere for 2 hours. The mixture was cooled to 25° C. for 1 hour, followed by the addition of concentrated H2SO4 (50 mL). The resulting syrup was poured onto ice and the pH was adjusted to 10 with NaOH (1M). The resulting solution was extracted with CHCl3, dried (Na2SO4) and evaporated to yield a brown liquid (1.56 g). This material was chromatographed according to Still et al. (J. Org. Chem., 1978, 43, 2923) on silica gel in EtOAc to yield 3 as a yellow liquid (1.4 g).

後処理

  1. customThe synthesis of 3
  2. temperatureThe mixture was cooled to 25° C. for 1 hour
  3. additionThe resulting syrup was poured onto ice
  4. extractionThe resulting solution was extracted with CHCl3
  5. dry with materialdried (Na2SO4)
  6. customevaporated

出典と根拠

ORDレコード
ord-2b3dea73df714fad9fc6ff59b1eabd1d
出典データセット
uspto-grants-1995_03
特許番号
US05395932

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