반응 #2383778

ord-1047302d657c4c47b2d228796d2cf922

반응 방정식

C1CCOC1
tetrahydrofuran
O=C1C=CC(=O)O1
maleic anhydride
C=C1CC2C=CC1C2.O=C1C=CC(=O)O1
5-methylenebicyclo[2.2.1]hept-2-ene maleic anhydride
수율 183.7%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타equipped with a thermometer, a condenser pipe, and a nitrogen inlet pipe
  2. 2
    온도the mixture was heated
  3. 3
    온도under reflux at 70 C
  4. 4
    workup.ADDITIONwhile introducing nitrogen for 8 hr
  5. 5
    기타polymerization
  6. 6
    기타After the completion of the polymerization
  7. 7
    기타to precipitate the resultant polymer, which
  8. 8
    기타was then dried

실험 절차

This synthesis example is directed to the synthesis of polymer (1b) (illustrated below as chemical formulas 14 or 15), a γ-hydroxy carboxylic acid structure. 21.2 g of 5-ethylenebicyclo[2.2.1]hept-2-ene, 19.6 g of maleic anhydride, 2.56 g of 2,2′-azobisisobutyronitrile, and 240 g of tetrahydrofuran were placed in a 500-ml, three-necked flask equipped with a thermometer, a condenser pipe, and a nitrogen inlet pipe, and the mixture was heated under reflux at 70 C. while introducing nitrogen for 8 hr to conduct polymerization. After the completion of the polymerization, the reaction mixture was poured into 1000 ml of n-hexane to precipitate the resultant polymer, which was then dried to give 37.5 g of a 5-methylenebicyclo[2.2.1]hept-2-ene/maleic anhydride copolymer (1a) (yield 92%). The polymer was analyzed by various methods and was found to mainly have a structure represented by the following formula:

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06489082B1uspto-grants-2002_12