반응 #992699

ord-6be066e91ff44d3aaf194c4243843944

반응 방정식

Cc1cccc(C)c1[N+](=O)[O-]
1,3-dimethyl-2-nitrobenzene
O=C(Cl)C(=O)Cl
oxalyl chloride
Cc1cccc(CC(=O)O)c1[N+](=O)[O-]
3-methyl-2-nitrobenzeneacetic acid
Cc1cccc(CC(=O)NC(C)C)c1[N+](=O)[O-]
title compound
Cc1cccc(CC(=O)NC(C)C)c1[N+](=O)[O-]
3-methyl-N-(1-methylethyl)-2-nitrobenzeneacetamide

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타resulting in a solution
  2. 2
    기타The volatiles were removed with a rotary evaporator
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in 10 mL of dichloromethane
  4. 4
    workup.ADDITIONHalf of this material was added dropwise at 0° C. to isopropylamine (1 mL) in 5 mL of dichloromethane
  5. 5
    workup.STIRRINGThe reaction mixture was stirred overnight at room temperature
  6. 6
    workup.ADDITIONSaturated sodium bicarbonate solution was added
  7. 7
    기타The solvent was removed with a rotary evaporator

실험 절차

To a slurry of 3-methyl-2-nitrobenzeneacetic acid (prepared by the method of H. Rapoport et al., J. Org. Chem., 1954, 77, 670-675 from 1,3-dimethyl-2-nitrobenzene, 0.70 g, 3.6 mmol) in 10 mL of dichloromethane was added oxalyl chloride (0.41 mL, 4.7 mmol) and two drops of N,N-dimethylformamide. The reaction mixture was stirred for 20 minutes, resulting in a solution. The volatiles were removed with a rotary evaporator. The residue was dissolved in 10 mL of dichloromethane. Half of this material was added dropwise at 0° C. to isopropylamine (1 mL) in 5 mL of dichloromethane. The reaction mixture was stirred overnight at room temperature. Saturated sodium bicarbonate solution was added, and the reaction mixture was passed through a Celite® diatomaceous filter aid cartridge. The solvent was removed with a rotary evaporator to afford the title compound as an orange solid (0.40 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08012499B2uspto-grants-2011_09