Sodium Iodide → HCID 53645944、化合物

HRID 1779789ノート

反応式

HRID 1779789 の反応式
[OH:1][C:2]1[CH:10]=[C:9]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH2:15](Br)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[I-].[Na+]>CC(C)=O>[CH2:15]([O:5][C:4](=[O:6])[C:3]1[CH:7]=[CH:8][C:9]([C:11]([CH3:14])([CH3:13])[CH3:12])=[CH:10][C:2]=1[O:1][CH2:4][C:3]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:2]=1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

参加物

6

反応物 4

HCID 5238Sodium IodideHCID 7498Benzyl BromideHCID 10796Cesium carbonateHCID 4330244-tert-Butyl-2-hydroxybenzoic acid

生成物 1

HCID 53645944HCID 53645944、化合物

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A mixture of 5 g of 2-hydroxy-4-tert-butyl-benzoic acid, 9.1 ml of benzyl bromide, 17 g of caesium carbonate, 0.3 g of sodium iodide and 500 ml of acetone is stirred for 20 hours under reflux and then filtered and the filtrate is concentrated by evaporation. The residue is partitioned between diethyl ether and water, the organic phases are concentrated by evaporation and the residue is purified by means of FC (1000 g of silica gel, dichloromethane/hexane=1:1). Title compound: Rf (dichloromethane/hexane=1:1)=0.47.

後処理

  1. temperatureunder reflux
  2. filtrationfiltered
  3. concentrationthe filtrate is concentrated by evaporation
  4. customThe residue is partitioned between diethyl ether and water
  5. concentrationthe organic phases are concentrated by evaporation
  6. customthe residue is purified by means of FC (1000 g of silica gel, dichloromethane/hexane=1:1)

出典と根拠

ORDレコード
ord-6c8ec676ea8c4f73b224da46c64386b0
出典データセット
uspto-grants-1997_05
特許番号
US05627182

反応ノート

読み込み中…