반응 #46962

ord-cfa93898b13c4cddbdf0bab68e95b661

반응 방정식

Cl
hydrochloride
CCCCC1=NC2(CCCC2)C(=O)N1
2-butyl-1,3-diazaspiro[4,4]non-1-en-4-one
[K+].[OH-]
potassium hydroxide
BrCc1ccc(I)cc1
4-iodobenzyl bromide
CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(I)cc1
title compound
수율 88.0%
CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(I)cc1
2-butyl-3-(4′-iodobenzyl)-1,3-diazaspiro[4,4]non-1-en-4-one
수율 88.0%

반응 조건

온도
25°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the mixture is heated
  2. 2
    온도at reflux for 1 hr
  3. 3
    기타the phases are separated
  4. 4
    workup.ADDITIONTo the organic phase is added 10 mL of concentrated hydrochloric acid, 100 mL
  5. 5
    기타is evaporated at reduced pressure, 300 mL of ethyl acetate
  6. 6
    workup.ADDITIONis added
  7. 7
    여과the resulting solid is filtered

실험 절차

A solution of 23.07 g (100 mmol) of the hydrochloride of 2-butyl-1,3-diazaspiro[4,4]non-1-en-4-one and 19.8 g of potassium hydroxide in 100 mL de water is added to a solution of 29.7 g (100 mmol) of 4-iodobenzyl bromide and 3.4 g (10 mmol) of tetrabutylammonium bisulphate in 30 mL of toluene, and the mixture is heated at reflux for 1 hr. After cooling to 25° C., 100 mL of water is added and the phases are separated. To the organic phase is added 10 mL of concentrated hydrochloric acid, 100 mL is evaporated at reduced pressure, 300 mL of ethyl acetate is added and the resulting solid is filtered to give 39.6 g (88%) of the title compound in the form of hydrochloride.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741492B2uspto-grants-2010_06