Réaction #2075737

ord-20223ad5f898485caa3e67541fb9ed32

Équation de réaction

CI
Iodomethane
CN(C)C=O
DMF
Cc1c(C(=O)O)cccc1[N+](=O)[O-]
2-methyl-3-nitrobenzoic acid
COC(=O)c1cccc([N+](=O)[O-])c1C
methyl 2-methyl-3-nitrobenzoate
Rendement 100.0%

Solvants

Conditions de réaction

Température
40°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Filtrationthe resulting precipitate collected by filtration
  2. 2
    Séchagedried over P2O5

Mode opératoire

With reference to FIG. 4, DMF (130 mL) was added to a well mixed 2-methyl-3-nitrobenzoic acid 2 (50 g, 0.28 mol) and KHCO3 (84 g, 0.84 mol) solution. Since the mixture became highly viscous, it was heated to 40° C. with manual shaking. Iodomethane (79 g, 0.56 mol) was added via syringe after the gas evolution had ceased. The resulting orange colored solution was stirred for 12 hours at room temperature. The reaction mixture was poured into water (800 mL), and the resulting precipitate collected by filtration and dried over P2O5 to give pure methyl 2-methyl-3-nitrobenzoate 3 (56 g, 100%) as a white solid: mp. 64.2-65.5° C.; 1H-NMR (CDCl3) δ 8.00 (d, J=7.8 Hz, 1H), 7.85 (d, J=8.0 Hz, 1H), 7.39 (t, J=8.0 Hz, 1H), 3.95 (s, 3H), 2.63 (s, 3H); IR (KBr, cm−1) 1724, 1548, 1279; MS (EI): 195 (M+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07642231B2uspto-grants-2010_01