반응 #1066149

ord-a14cc1244ab845b09a26a6d7298f3efc

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타was quantitatively formed
  2. 2
    기타After the amine salt was removed by filtration
  3. 3
    기타the solvent and excess pyridine were evaporated
  4. 4
    기타The intended product was obtained as a syrup
  5. 5
    기타An attempt to recrystallize it from ether and n-hexane
  6. 6
    기타failed, since hydrolysis
  7. 7
    기타contained in the solvents for recrystallization

실험 절차

The procedure of Example 2 was repeated except that 3.96 g (0.05 mol) of dry pyridine was used in place of triethylamine and the reaction was carried out in THF. It was confirmed when the reaction solution was examined by means of thin-layer chromatography that triphenylmethyl methacrylate was quantitatively formed. After the amine salt was removed by filtration, the solvent and excess pyridine were evaporated. The intended product was obtained as a syrup. An attempt to recrystallize it from ether and n-hexane failed, since hydrolysis took place due to water contained in the solvents for recrystallization and triphenylmethyl alcohol was formed.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04666633uspto-grants-1987_05