Reaction #1178419

ord-3ae3317de4f3437a8d50821e23ccf160

Reaction equation

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
Yield 101.2%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.STIRRINGthe mixture was stirred for 0.5 h
  2. 2
    ExtractionThe mixture was extracted with ether (150 mL)
  3. 3
    ExtractionThe ether extract
  4. 4
    Washwas washed with saturated aqueous NaHCO3 (50 mL)
  5. 5
    Otherdried
  6. 6
    Otherevaporated under reduced pressure

Procedure

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08129355B2uspto-grants-2012_03