Water → HCID 57545186、化合物

HRID 1661518ノート

反応式

HRID 1661518 の反応式
C[O:2][C:3](=[O:25])[CH:4]([C:18]1[CH:23]=[CH:22][C:21]([Br:24])=[CH:20][CH:19]=1)[O:5][C:6]1[CH:11]=[C:10]([O:12][CH2:13][CH3:14])[CH:9]=[C:8]([O:15][CH2:16][CH3:17])[CH:7]=1.O.C(=O)([O-])[O-].[K+].[K+]>CO>[Br:24][C:21]1[CH:20]=[CH:19][C:18]([CH:4]([O:5][C:6]2[CH:7]=[C:8]([O:15][CH2:16][CH3:17])[CH:9]=[C:10]([O:12][CH2:13][CH3:14])[CH:11]=2)[C:3]([OH:25])=[O:2])=[CH:23][CH:22]=1

参加物

5

実験手順

16.9 g (41.3 mmol) of methyl(4-bromophenyl)-(3,5-diethoxyphenoxy)acetate are dissolved in 80 ml of methanol and 8 ml of water under argon at RT, and 7.99 g (57.8 mmol) of potassium carbonate are added. The mixture is heated under RF for 4 h. After cooling, the precipitate is filtered off, the filtrate is concentrated, the residue is taken up in water and the solution is extracted four times with diethyl ether. The aqueous phase is adjusted to a pH of 2 by adding 10% strength hydrochloric acid and is extracted three times with ethyl acetate, and the combined ethyl acetate phases are washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated. 16.1 g (99% of theory) of the product are obtained.

後処理

  1. temperatureThe mixture is heated under RF for 4 h
  2. temperatureAfter cooling
  3. filtrationthe precipitate is filtered off
  4. concentrationthe filtrate is concentrated
  5. extractionthe solution is extracted four times with diethyl ether
  6. additionby adding 10% strength hydrochloric acid
  7. extractionis extracted three times with ethyl acetate
  8. washthe combined ethyl acetate phases are washed with saturated sodium chloride solution
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated
  12. custom16.1 g (99% of theory) of the product are obtained

出典と根拠

ORDレコード
ord-19482c96379b47138c2ad592573849b3
出典データセット
uspto-grants-2011_10
特許番号
US08030347B2

反応ノート

読み込み中…