p-Toluenesulfonic acid monohydrate → 2-(3-Nitro-6-fluorophenyl)-5-methylbenzoxazole
Reaction equation
O[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[NH:9][C:10](=[O:21])[C:11]1[CH:16]=[C:15]([N+:17]([O-:19])=[O:18])[CH:14]=[CH:13][C:12]=1[F:20].O.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[N+:17]([C:15]1[CH:16]=[C:11]([C:10]2[O:21][C:2]3[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=3[N:9]=2)[C:12]([F:20])=[CH:13][CH:14]=1)([O-:19])=[O:18]Participants
3
Procedure
Prepared by the method of Example 15b), from N-(2-hydroxy-5-methylphenyl)-2-fluoro-5-nitrobenzamide (667 mg, 2.3 mmol) and p-toluenesulfonic acid monohydrate (961 g, 5.1 mmol) the subtitle compound was obtained (345 mg, 55%). 1H NMR (DMSO) δ 8.92(m, 1H), 8.50(m, 1H), 7.79(t, 1H), 7.67(d, 1H), 7.39(t, 1H), 7.28(d, 1H), 2.60(s, 3H).
Sources & evidence
- ORD record
- ord-bfb16d589aed4e8f95b125fd57d6e2d2
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07138425B2
Reaction notes
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