反应 #1178419

ord-3ae3317de4f3437a8d50821e23ccf160

反应方程式

O=S([O-])([O-])=S.[Na+].[Na+]
Na2S2O3
O=C([O-])O.[Na+]
NaHCO3
COc1cccc(C(=O)NC(C)(CO)C(C)C)c1C
N-(1-hydroxymethyl-1,2-dimethyl-propyl)-3-methoxy-2-methyl-benzamide
CC(=O)OI1(OC(C)=O)(OC(C)=O)OC(=O)c2ccccc21
Dess-Martin periodinane
COc1cccc(C(=O)NC(C)(C=O)C(C)C)c1C
N-(1-formyl-1,2-dimethyl-propyl)-3-methoxy-2-methyl-benzamide
收率 101.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGthe mixture was stirred for 0.5 h
  2. 2
    萃取The mixture was extracted with ether (150 mL)
  3. 3
    萃取The ether extract
  4. 4
    洗涤was washed with saturated aqueous NaHCO3 (50 mL)
  5. 5
    其他dried
  6. 6
    其他evaporated under reduced pressure

实验过程

To a stirred solution of N-(1-hydroxymethyl-1,2-dimethyl-propyl)-3-methoxy-2-methyl-benzamide (X, R1=2-Me-3-MeO-Ph, R2=i-Pr, R3=Me, 285 mg, 1.1 mmol) in CH2Cl2 (10 mL) at room temperature was added Dess-Martin periodinane solution (15% by weight, 2.4 mL, ca. 1.1 mmol). The mixture was stirred at room temperature for 4 h and poured into saturated aqueous NaHCO3 (50 mL). Solid Na2S2O3 (2.13 g, 8.6 mmol) was added and the mixture was stirred for 0.5 h. The mixture was extracted with ether (150 mL). The ether extract was washed with saturated aqueous NaHCO3 (50 mL), dried and evaporated under reduced pressure to afford N-(1-formyl-1,2-dimethyl-propyl)-3-methoxy-2-methyl-benzamide (293 mg) as an oil. 1H NMR (CDCl3) δ (ppm): 0.98 (d, J=6.6 Hz, 3H), 1.04 (d, J=6.6 Hz, 3H), 1.51 (s, 3H), 2.27 (s, 3H), 2.29 (m, 1H), 3.84 (s, 3H), 6.30 (br s, 1H), 6.91 (m, 1H), 6.96 (m, 1H), 7.18 (m, 1H), 9.60 (s, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08129355B2uspto-grants-2012_03