반응 #215696

ord-37dd6bbf2b0c4f0ea822e3721e35198b

반응 방정식

O=C1C=CC(=O)N1
maleimide
C=CC=CNC(=O)OC(C)(C)C
1-(tert.-butyloxycarbonylamino)-1,3-butadiene
CC(C)(C)OC(=O)NC1C=CCC2C(=O)NC(=O)C12
4-(tert.-Butyloxycarbonylamino)-1,3-dioxo-1,3,3a,4,7,7a-hexahydroisoindole

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타being kept at 20° to 30° C
  2. 2
    농축It is then concentrated
  3. 3
    기타the residue is recrystallised from ethyl acetate
  4. 4
    기타are obtained
  5. 5
    기타A further 13 g of melting point 158° to 160° C. are obtained from the mother liquor

실험 절차

48.0 g (0.5 mol) of maleimide are initially introduced into the reaction vessel as a solution in 200 ml of absolute tetrahydrofuran, and 120 g (0.5 mol) of approximately 70% strength 1-(tert.-butyloxycarbonylamino)-1,3-butadiene are added dropwise as a solution in 500 ml of absolute tetrahydrofuran, the temperature being kept at 20° to 30° C. The mixture is subsequently stirred overnight at room temperature. It is then concentrated and the residue is recrystallised from ethyl acetate. 57 g of product having a melting point of 177° to 182° C. are obtained. A further 13 g of melting point 158° to 160° C. are obtained from the mother liquor.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05464796uspto-grants-1995_11