반응 #214023

ord-2b2a6e5ae4814ff9a5a1ea69add86605

반응 방정식

O=C=O
carbon dioxide
N#CCC(=O)O
cyanoacetic acid
OC1(c2ccccc2)CCNCC1
4-hydroxy-4-phenylpiperidine
C=O
formaldehyde
C=C(C#N)CN1CCC(O)(c2ccccc2)CC1
2-[(4-Hydroxy-4-phenyl-1-piperidyl)methyl]propenenitrile

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도while maintaining an internal temperature of 20°-25° C
  2. 2
    workup.ADDITIONUpon complete addition
  3. 3
    workup.ADDITIONwas added dropwise in approximately five minutes
  4. 4
    기타was 28° C
  5. 5
    workup.ADDITIONmixed with 100 ml
  6. 6
    기타of methylene chloride, the organic phase separated
  7. 7
    세척washed with water and salt solution
  8. 8
    기타Upon removal of solvent the product
  9. 9
    기타was obtained as an oil, 10.5 g

실험 절차

A solution of cyanoacetic acid (4.3 g., 0.05 mole) in 15 ml. of dioxane was cooled with an ice bath, and 4-hydroxy-4-phenylpiperidine (8.8 g., 0.05 mole) added while maintaining an internal temperature of 20°-25° C. Upon complete addition and a further fifteen minutes of stirring 37% aqueous formaldehyde (9 gm., 0.10 mole) was added dropwise in approximately five minutes. When approximately half was added carbon dioxide evolution was observed, the maximum internal temperature was 28° C. The reaction mixture was stirred overnight, mixed with 100 ml. of methylene chloride, the organic phase separated washed with water and salt solution. Upon removal of solvent the product was obtained as an oil, 10.5 g., in practically analytical purity.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04254131uspto-grants-1981_03