Azobisisobutyronitrile → Styrene

HRID 32045

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HRID 32045 반응식
[C:1]1(=O)[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.[CH3:8][C:9]1(C)N([O])[C:13]([CH3:17])(C)[CH2:12][CH2:11][CH2:10]1.CC(N=NC(C#N)(C)C)(C#N)C>C=CC1C=CC=CC=1.C(OC(=O)C=C)CCC>[CH2:1]=[CH:2][C:3]1[CH:4]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH2:11]([O:6][C:4](=[O:5])[CH:3]=[CH2:2])[CH2:12][CH2:13][CH3:17]

참가 물질

6

반응물 3

HCID 6547AzobisisobutyronitrileHCID 7923Maleic Anhydride2회HCID 2724126Tempo

생성물 2

HCID 7501StyreneHCID 8846Butyl Acrylate

시약·촉매·용매 1

HCID 168422Butyl prop-2-enoate;styrene용매

반응 조건

온도
135 °C

실험 절차

Incorporation of maleic anhydride into an emulsion aggregation particle at the bulk polymerization step. A stock solution of styrene (390 mL) and butylacrylate (110 ml) was prepared and to 400 ml was added TEMPO (3.12 g, 0.02 mole) and vazo 64 initiator (2.0 g, 0.0125 mole). This was heated tinder a nitrogen atmosphere to 135° C. (bath temperature) and then added to it dropwise a solution of maleic anhydride (9.8 g) in 100 mL of the styrene/butylacrylate stock solution that had been deoxygenated using nitrogen. The addition was done over a 30 minute period after which it was stirred for 5 more minutes and then cooled to afford a poly(styrene/maleic anhydride-b-styrene/butylacrylate) (Mn=4,990 with PD=1.23) solution in styrene/butylacrylate monomer.

후처리

  1. customhad been deoxygenated
  2. additionThe addition
  3. temperaturecooled

출처 및 근거

ORD 기록
ord-4fb961fd634446639aca2f5016437d7d
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07426074B2

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