反応 #1435685

ord-9a303e2fe8484066b9459e7f74b8a489

反応方程式

COc1c(C)cc(N2CCOC2=O)cc1N1CCOC1=O
3,3′-(4-methoxy-5-methyl-1,3-phenylene)bis-(1,3-oxazolidin-2-one)
[K+].[OH-]
KOH
Cl
HCl
COc1c(C)cc(NCCO)cc1NCCO
2,4-Bis[(2-hydroxyethyl)amino]-6-methylanisole

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出extracted several times with ethyl acetate
  2. 2
    その他The combined ethyl acetate phases were evaporated on a Rotavapor
  3. 3
    workup.DISTILLATIONdistilled in a Kugelrohr (250–290° C., 0.08 mbar)

実験手順

33.5 g of 3,3′-(4-methoxy-5-methyl-1,3-phenylene)bis-(1,3-oxazolidin-2-one) were heated under reflux in 500 ml of 20% strength KOH for 10 h. The mixture was cooled to room temperature and poured onto 1.5 l of iced water. The mixture was then neutralized with HCl and extracted several times with ethyl acetate. The combined ethyl acetate phases were evaporated on a Rotavapor and then distilled in a Kugelrohr (250–290° C., 0.08 mbar).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07211119B2uspto-grants-2007_05