반응 #3008

ord-2778a9f71b614c56aa952dc1c3b7fac4

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The resulting clear solution was heated for 2-3 hours
  2. 2
    온도under reflux until it
  3. 3
    건조After drying over sodium sulphate the solution
  4. 4
    기타was strongly evaporated (residual volume ca. 50 ml) and it
  5. 5
    기타was crystallized

실험 절차

2 ml 3N HCl was added to a suspension of 8.0 g (30 mmol) 4-hydroxy-6-[2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]-2H-pyran-2-one VII and 300 ml tetrahydrofuran. The resulting clear solution was heated for 2-3 hours under reflux until it was no longer possible to detect starting material. (TLC control, mobile solvent: toluene/ethyl formate/methanol 5:4:1, 0.5% formic acid). After drying over sodium sulphate the solution was strongly evaporated (residual volume ca. 50 ml) and it was crystallized by admixing with ether. Yield 4.7 g (63%) hispidine II, melting point 232°-234° C. (decomp.) or melting point 253° C. (decomp; bunch of needles from toluene/ethyl formate).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05731344uspto-grants-1998_03