반응 #48232

ord-c05a971138724dfeb0aba79d83b73319

반응 방정식

CCCCCC.CCOC(C)=O
EtOAc n-hexane
COc1cc(C=O)ccc1O
vanillin
CN(C)S(=O)(=O)Cl
N,N-dimethylsulfamoyl chloride
COc1cc(C=O)ccc1S(=O)(=O)N(C)C
4-(N,N-Dimethylsulfamoyl)-3-methoxybenzaldehyde

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타transferred to a separating funnel
  2. 2
    세척The organic layer was washed with water (2×200 mL), 6M HCl (aq.) (200 mL), brine (2×200 mL)
  3. 3
    건조dried (Na2SO4)
  4. 4
    여과filtered
  5. 5
    농축Concentration in vacuo of the combined filtrates
  6. 6
    기타gave a golden-yellow oil which
  7. 7
    여과filtered
  8. 8
    기타air-dried
  9. 9
    기타to give OBS02011 as yellow plates (6.92 g, 89%)

실험 절차

To a solution of vanillin (4.56 g, 30 mmol) in N,N-dimethylcyclohexylamine (30 mL) at 80-90° C., was added N,N-dimethylsulfamoyl chloride (3.79 mL, 35.27 mmol). The mixture was stirred at this temperature for 4 h, transferred to a separating funnel and diluted with EtOAc (100 mL). The organic layer was washed with water (2×200 mL), 6M HCl (aq.) (200 mL), brine (2×200 mL), dried (Na2SO4) and filtered. Concentration in vacuo of the combined filtrates gave a golden-yellow oil which solidified on standing. The product was stirred in n-hexane, filtered and air-dried to give OBS02011 as yellow plates (6.92 g, 89%). TLC [SiO2, EtOAc-n-hexane (1:1)] Rf=0.65; 1H-NMR (270 MHz, CDCl3)=2.98 (6H, s), 3.93 (3H, s), 7.44 (1H, d, J=1.6), 7.48 (1H, dd, J=1.6, 8.1), 7.53 (1H, d, J=8.1), 9.92 (1H, s).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745472B2uspto-grants-2010_06