Vanillin → 4-(N,N-Dimethylsulfamoyl)-3-methoxybenzaldehyde

HRID 19954

반응식

HRID 19954 반응식
[O:1]=[CH:2][C:3]1[CH:11]=[CH:10][C:8](O)=[C:5]([O:6][CH3:7])[CH:4]=1.[CH3:12][N:13]([CH3:18])[S:14](Cl)(=[O:16])=[O:15].CCOC(C)=O.CCCCCC>CN(C1CCCCC1)C.CCOC(C)=O.CCCCCC>[CH3:12][N:13]([CH3:18])[S:14]([C:8]1[CH:10]=[CH:11][C:3]([CH:2]=[O:1])=[CH:4][C:5]=1[O:6][CH3:7])(=[O:16])=[O:15]

참가 물질

7

반응물 3

HCID 1183VanillinHCID 83372Dimethylsulphamoyl chlorideHCID 21226206Ethyl acetate hexane

생성물 1

HCID 219768714-(N,N-Dimethylsulfamoyl)-3-methoxybenzaldehyde

시약·촉매·용매 3

HCID 7415N,N-Dimethylcyclohexylamine용매HCID 8058Hexane용매HCID 8857Ethyl Acetate용매

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).

후처리

  1. customtransferred to a separating funnel
  2. washThe organic layer was washed with water (2×200 mL), 6M HCl (aq.) (200 mL), brine (2×200 mL)
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationConcentration in vacuo of the combined filtrates
  6. customgave a golden-yellow oil which
  7. filtrationfiltered
  8. customair-dried
  9. customto give OBS02011 as yellow plates (6.92 g, 89%)

출처 및 근거

ORD 기록
ord-c05a971138724dfeb0aba79d83b73319
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07745472B2

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