반응 #54241

ord-da22df0d8761434b9bbdfb30e3940d12

반응 방정식

O=C1C=CC=C2OCC=C12
cyclohexa(b)furan-4-one
[C-]#N.[K+]
potassium cyanide
O=C([O-])[O-].[NH4+].[NH4+]
ammonium carbonate
O
water
Cl
hydrochloric acid
O=C1NC(=O)C2(C=CC=C3OCC=C32)N1
spiro[cyclohexa(b)furan-4,4'-imidazolidine]-2', 5'-dione

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction mixture was cooled
  2. 2
    기타The precipitated product was isolated by filtration
  3. 3
    기타recrystallized from ethanol

실험 절차

A mixture of 2.7 g of cyclohexa(b)furan-4-one (Bull. Soc. Chim. Fr., 1967, 2796), 1.95 g of potassium cyanide and 9.6 g of powdered ammonium carbonate were heated with 40 ml of 95% aqueous ethanol at 110°-120° C. in a steel bomb for 16 hours. The reaction mixture was cooled, diluted with 200 ml of water, and acidified with 12 N hydrochloric acid. The precipitated product was isolated by filtration and recrystallized from ethanol to give 1.73 g of spiro[cyclohexa(b)furan-4,4'-imidazolidine]-2', 5'-dione, mp 245°-248° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04147797uspto-grants-1979_04