반응 #4589

ord-dc25777ecaf7489698498252fb79841d

반응 방정식

CCCCCCCCCCCCCCCCCC(=O)Cl
Stearoyl chloride
N#CN.[Na]
sodium cyanamide
C
charcoal
CCCCCCCCCCCCCCCCCC(=O)NC#N
Stearoylcyanamide
수율 92.4%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added drop-wise
  2. 2
    workup.DISTILLATIONof freshly distilled dry THF with vigorous stirring
  3. 3
    기타The solids which formed
  4. 4
    여과were collected by filtration
  5. 5
    여과filtered
  6. 6
    기타air-dried
  7. 7
    기타to give 2.85 g (92.4% yield) of crude 7
  8. 8
    농축The filtrate was concentrated until the solution
  9. 9
    workup.ADDITIONAddition of petroleum ether
  10. 10
    기타gave 2.29 g (crop 1) of white waxy 7
  11. 11
    농축The filtrate was concentrated
  12. 12
    workup.ADDITIONpetroleum ether added
  13. 13
    기타to give 0.28 g (crop 2) of additional product
  14. 14
    기타giving a total yield of 83.3%, mp 74°-75 ° C
  15. 15
    기타quenching (weak)
  16. 16
    기타no color reaction with ferricyanide spray reagent

실험 절차

Stearoyl chloride (3.03 g, 0.010 mol) in 50 ml of freshly distilled dry THF was added drop-wise to a suspension of sodium cyanamide (1.92 g, 0.030 mol) in 100 ml of freshly distilled dry THF with vigorous stirring. The reaction was allowed to proceed at 25° C for 63 hours. The solids which formed were collected by filtration and the solid cake was suspended in 200 ml of distilled water. The resulting soapy suspension (pH 10.5) was acidified to pH 1.5 with 10% HCl, filtered, and air-dried to give 2.85 g (92.4% yield) of crude 7. This was dissolved in THF and the solution decolorized with activated charcoal. The filtrate was concentrated until the solution became turbid. Addition of petroleum ether gave 2.29 g (crop 1) of white waxy 7. The filtrate was concentrated and petroleum ether added to give 0.28 g (crop 2) of additional product giving a total yield of 83.3%, mp 74°-75 ° C. TLC: Rf =0.69 in EtOAc/petroleum ether/AcOH (50:100:1), detected by UV quenching (weak) and no color reaction with ferricyanide spray reagent; IR (Nujol, cm-1) 3210 (NH), 2250 (C≡N), 1735 (C=O); NMR (Silanor C, δ from TMS) 2.3-2.6 (t, --CH2 --CH2 --C=O), 1.0-1.8 (fused s, (CH2)14), 0.8-0.9 (t, CH3 --CH2 --); Anal. Calcd for C19H36N2O: C, 73.97; H, 11.76; N, 9.08. Found: C, 73.88; H, 11.50; N, 9.09.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04726941uspto-grants-1988_02