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

HRID 386316

反応式

HRID 386316 の反応式
C(OC(C)COC)(=O)C.N(C(C)(C)C#N)=NC(C)(C)C#N.[CH2:22]=[CH:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.[C:30]([OH:34])(=[O:33])[CH:31]=[CH2:32]>>[CH:22]([CH:32]=[CH:31][C:30]([OH:34])=[O:33])=[CH:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

参加物

5

反応物 4

HCID 6547AzobisisobutyronitrileHCID 6581Acrylic AcidHCID 7501StyreneHCID 7946Propylene glycol methyl ether acetate

生成物 1

HCID 737775-Phenyl-2,4-pentadienoic acid

実験手順

432 g of propyleneglycol monomethyl ether acetate and 13 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 96.3 g of styrene and 11.8 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, 6.5 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 3000.

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-228c2b448f2f4349b845dab6dcb7f5d6
出典データセット
uspto-grants-2013_02
特許番号
US08368851B2

関連ノート

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