Methanol → p-Tert-butoxystyrene cyclohexyl acrylate

HRID 237189

反応式

HRID 237189 の反応式
[C:1]([O:5][C:6]1[CH:13]=[CH:12][C:9]([CH:10]=[CH2:11])=[CH:8][CH:7]=1)([CH3:4])([CH3:3])[CH3:2].[C:14]([O:18][CH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1)(=[O:17])[CH:15]=[CH2:16].N(C(C)(C)C#N)=NC(C)(C)C#N.CO>C(O)(C)C>[C:1]([O:5][C:6]1[CH:7]=[CH:8][C:9]([CH:10]=[CH2:11])=[CH:12][CH:13]=1)([CH3:4])([CH3:2])[CH3:3].[C:14]([O:18][CH:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]1)(=[O:17])[CH:15]=[CH2:16]

参加物

6

反応物 4

HCID 887MethanolHCID 6547AzobisisobutyronitrileHCID 18298Cyclohexyl acrylateHCID 5775311-(Tert-butoxy)-4-ethenylbenzene

生成物 1

HCID 86587325p-Tert-butoxystyrene cyclohexyl acrylate

試薬・触媒・溶媒 1

HCID 3776Isopropanol溶媒

反応条件

温度
75 °C

実験手順

First, 176.3 g (1.0 mol) of p-tert-butoxystyrene and 16.2 g (0.105 mol) of cyclohexyl acrylate were dissolved in 250 ml of isopropanol. In a nitrogen stream, 2,2′-azobisisobutyronitrile was added to the solution, and agitated at 75° C. for six hours. The reaction liquid was cooled, and poured in 5000 ml of an aqueous solution of methanol, thereby precipitating a reaction product. The precipitated solid was collected by filtration, washed with methanol, and dried in vacuum. Thus, 172.5 g of poly(p-tert-butoxystyrene/cyclohexyl acrylate) was obtained as a white powdery crystal.

後処理

  1. customThe reaction liquid
  2. temperaturewas cooled
  3. customprecipitating a reaction product
  4. filtrationThe precipitated solid was collected by filtration
  5. washwashed with methanol
  6. customdried in vacuum

出典と根拠

ORDレコード
ord-fd69cfff23654517bbdcb8f85511322a
出典データセット
uspto-grants-2014_02
特許番号
US08642245B2

関連ノート

読み込み中…