반응 #71315

ord-818b5de95ec84349a493cb973336f9b6

반응 방정식

Cc1ccccc1
toluene
C=CC(=O)OCCCC
N-butyl acrylate
C=C(C)C(=O)OCC1CO1
glycidyl methacrylate
CCCCCCCCCCCCS
lauryl mercaptan
C=C(C)C(=O)OCC1CO1.C=CC(=O)OCCCC
copolymer ( B8 )
C=C(C)C(=O)OCC1CO1.C=CC(=O)OCCCC
glycidyl methacrylate n-butyl acrylate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타equipped with a stirrer, a condenser
  2. 2
    workup.ADDITIONa thermometer, and a nitrogen gas-introducing inlet, and mixed
  3. 3
    기타to give a monomer mixture solution
  4. 4
    기타The obtained monomer mixture solution was bubbled with nitrogen gas for 20 minutes
  5. 5
    기타to remove the dissolved oxygen
  6. 6
    온도the temperature inside the separable flask was raised to a reflux temperature
  7. 7
    기타Next, polymerization
  8. 8
    기타in Synthesis Example 6

실험 절차

50 g of N-butyl acrylate (product of Nippon Shokubai Co., Ltd.), 50 g of glycidyl methacrylate (product of Mitsubishi Gas Chemical Company Inc.), 3 g of lauryl mercaptan (product of Wako Pure Chemical Industries Ltd.), and 100 g of toluene were placed in a 1 L-separable flask equipped with a stirrer, a condenser, a thermometer, and a nitrogen gas-introducing inlet, and mixed to give a monomer mixture solution. The obtained monomer mixture solution was bubbled with nitrogen gas for 20 minutes to remove the dissolved oxygen. Thereafter, the system in the separable flask was replaced with nitrogen gas, and the temperature inside the separable flask was raised to a reflux temperature under stirring. Next, polymerization was performed in the same manner as that in Synthesis Example 6 to provide a toluene/ethanol solution of a poly(glycidyl methacrylate/n-butyl acrylate) copolymer (B8) (number-average molecular weight of 3,000 as converted to polystyrene, epoxide equivalent of 284) as a curable compound having at least two glycidyl groups.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08536242B2uspto-grants-2013_09