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Azobisisobutyronitrile → 5-Phenyl-2,4-pentadienoic acid

HRID 386314
ノート
印刷プレビュー

反応式

HRID 386314 の反応式
C1(=O)CCCCC1.N(C(C)(C)C#N)=NC(C)(C)C#N.[CH2:20]=[CH:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.[C:28]([OH:32])(=[O:31])[CH:29]=[CH2:30]>>[CH:20]([CH:30]=[CH:29][C:28]([OH:32])=[O:31])=[CH:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 6547AzobisisobutyronitrileHCID 6581Acrylic AcidHCID 7501StyreneHCID 7967Cyclohexanone

生成物 1

HCID 737775-Phenyl-2,4-pentadienoic acid

実験手順

432 g of cyclohexanone and 3 g of azobisisobutyronitrile were poured into a five-necked reaction vessel having a capacity of one litter. Then, while introducing nitrogen gas into the reaction vessel, the resultant mixture was heated to 80° C. Then, a mixed liquid constituted by 98.9 g of styrene and 9.1 g of acrylic acid was added drop-wise to the above mixture taking two hours. 30 minutes after finishing of the dropping of the mixed liquid, 3 g of azoisobutyronitrile was added to the resultant mixture and the mixture thus obtained was heated for 5 hours to obtain a styrene-acrylic acid copolymer. The weight average molecular weight of the styrene-acrylic acid copolymer thus obtained was 6900.

後処理

  1. additionThen, while introducing nitrogen gas into the reaction vessel
  2. additionwas added drop-wise to the above mixture
  3. custom30 minutes
  4. customthe mixture thus obtained
  5. temperaturewas heated for 5 hours

出典と根拠

ORDレコード
ord-5e56cc0833d64890b2786927ffe692d2
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08368851B2

反応ノート

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