반응 #445975

ord-31efc3a66a4f4a569fa7ab4020729223

반응 방정식

C=CN1CCCC1=O
N-vinylpyrrolidinone
C=CC(=O)NCCCCCCCC
N-1-octylacrylamide
Cl.Cl.Nc1c(F)c(N)c(F)c(F)c1F
dihydrochloride
CCCCCCCCCCCCOS(=O)(=O)[O-].[Na+]
sodium dodecylsulfate
C=CC(=O)NCCCCCCCC.C=CC(N)=O.C=CN1CCCC1=O.CC(=O)N(C)C
N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타fitted with a chilled water condenser
  2. 2
    기타The temperature was adjusted to 25 C and polymerization
  3. 3
    여과filtered
  4. 4
    기타dried under vacuum at 30° C

실험 절차

A solution was prepared of 3.0 g of sodium dodecylsulfate in 300 mL of deoxygenated water. N-1-octylacrylamide, 0.597 g, was dissolved in this solution folloW®d by 18.30 g of acrylamide, 19.38 g of DMA and 2I.73 g of N-vinylpyrrolidinone (NVP). The resulting solution was carefully transferred to a 1 L Morton style resin kettle fitted with a chilled water condenser, thermometer, inert gas sparger and mechanical stirrer. The temperature was adjusted to 25 C and polymerization was initiated by the addition of 0.108 g of 2,2'-azobis(N,N,--dimethylene-isobutyramidine) dihydrochloride. After stirring for 16 hr at 25°±0.2° C., a 250 mL portion of the viscous solution was added to 3 L of acetone. The precipitated polymer was then masticated in a Waring blender with methanol/acetone, filtered and dried under vacuum at 30° C. The yield of polymer was 55.53 g. Other examples of these polymers are given in Table III.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04997878uspto-grants-1991_03