Sodium Carbonate → 4-Chloro-6-(2,6-diethylphenyl)-2-trifluoromethyl-nicotinic acid methyl ester

HRID 251589Notes

Reaction equation

HRID 251589 reaction equation
[CH3:1][O:2][C:3](=[O:16])[C:4]1[C:9]([Cl:10])=[CH:8][C:7](Cl)=[N:6][C:5]=1[C:12]([F:15])([F:14])[F:13].[CH2:17]([C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([CH2:25][CH3:26])[C:20]=1B(O)O)[CH3:18].C(=O)([O-])[O-].[Na+].[Na+]>C1(C)C=CC=CC=1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:1][O:2][C:3](=[O:16])[C:4]1[C:9]([Cl:10])=[CH:8][C:7]([C:20]2[C:21]([CH2:25][CH3:26])=[CH:22][CH:23]=[CH:24][C:19]=2[CH2:17][CH3:18])=[N:6][C:5]=1[C:12]([F:15])([F:14])[F:13]

Participants

6

Procedure

A mixture of 4,6-dichloro-2-trifluoromethyl-nicotinic acid methyl ester (1.0 g, 3.7 mmol), 2,6-diethyl-phenyl boronic acid (0.78 g, 4.4 mmol), sodium carbonate (2 M aqueous solution, 4.4 mL, 8.8 mmol), and Pd(PPh3)4 (206 mg, 0.18 mmol) is refluxed in toluene for 48 hours and then cooled to room temperature. The organic layer is separated and the aqueous layer is extracted with ethyl acetate (2×50 mL). The combined organic layers are dried and the solvent removed. The crude product is purified by flash column (hexanes/ethyl acetate 8:1) to give 4-chloro-6-(2,6-diethylphenyl)-2-trifluoromethyl-nicotinic acid methyl ester as a white solid. 1H NMR: (CDCl3) 7.58 (s, 1H), 7.25 (t, 1H), 7.20 (d, 2H), 4.02 (s, 2.28 (q, 4H), 1.04 (t, 6H).

Workup

  1. customThe organic layer is separated
  2. extractionthe aqueous layer is extracted with ethyl acetate (2×50 mL)
  3. customThe combined organic layers are dried
  4. customthe solvent removed
  5. customThe crude product is purified by flash column (hexanes/ethyl acetate 8:1)

Sources & evidence

ORD record
ord-19ed12c927db43759386f34385e34728
Source dataset
uspto-grants-2011_01
Patent number
US07863454B2

Reaction notes

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