Ethyl bromoacetate → 3-(2',4'-Dibromo-4-biphenylyl)-3-hydroxybutyric acid ethyl ester

HRID 26912ノート

反応式

HRID 26912 の反応式
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][C:11]=2[Br:17])=[CH:6][CH:5]=1)(=[O:3])[CH3:2].Br[CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21]>>[CH2:23]([O:22][C:20](=[O:21])[CH2:19][C:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][C:11]=2[Br:17])=[CH:6][CH:5]=1)([OH:3])[CH3:2])[CH3:24]

参加物

3

実験手順

3.44 g. of 4-acetyl-2',4'-dibromobiphenyl and 1.5 g. of ethyl bromoacetate are added to a mixture of 6.5 g. of granulated zinc, previously washed with dilute hydrochloric acid, water and acetone and dried, and 0.2 g. of iodine in 70 ml. of benzene and 70 ml. of diethyl ether. The mixture is heated under reflux for 4 hours with occasional shaking. 5 g. of zinc and a trace of iodine are added after 1, 2 and 3 hours, respectively, and 1.5 g. of ethyl bromoacetate added after 2 hours. After cooling, acetic acid is added to decompose the resulting alcoholate and methanol is added to bring the product into solution. The mixture is poured into water and the organic phase is separated off and worked up to give 3-(2',4'-dibromo-4-biphenylyl)-3-hydroxybutyric acid ethyl ester.

後処理

  1. washof granulated zinc, previously washed with dilute hydrochloric acid, water and acetone
  2. customdried
  3. temperatureThe mixture is heated
  4. temperatureunder reflux for 4 hours with occasional shaking
  5. additionof zinc and a trace of iodine are added after 1, 2 and 3 hours
  6. additionof ethyl bromoacetate added after 2 hours
  7. temperatureAfter cooling
  8. additionacetic acid is added
  9. additionis added
  10. additionThe mixture is poured into water
  11. customthe organic phase is separated off

出典と根拠

ORDレコード
ord-c8fc1294a2aa4b3ea72202720ae56cda
出典データセット
uspto-grants-1979_04
特許番号
US04151302

反応ノート

読み込み中…