Water → 1-Methoxy-2-methyl-4-nitrobenzene

HRID 866006

Reaction equation

HRID 866006 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH3:9].F[B-](F)(F)F.[O:15]=[N+:16]=[O:17].O>ClCCl>[CH3:1][C:2]1[CH:7]=[C:6]([N+:16]([O-:17])=[O:15])[CH:5]=[CH:4][C:3]=1[O:8][CH3:9]

Participants

5

Procedure

2-Methylanisole (20 g) in 500 ml dichloromethane chilled in an ice bath is treated with 27.2 g of nitronium tetrafluoroborate and stirred two days. The mixture is poured into water, the layers are separated, and the aqueous phase is washed with dichloromethane. The combined organic layers are dried, filtered, stripped, and chromatographed on silica gel with 9:1 to 8:2 hexane:ethyl acetate to give 2-methyl-4-nitroanisole. NMR (CDCl3): δ2.3 (3H,s), 3.9 (3H,s), 6.9 (1H,d), 8.0 (1H,d), 8.1 (1H,d of d).

Workup

  1. customthe layers are separated
  2. washthe aqueous phase is washed with dichloromethane
  3. customThe combined organic layers are dried
  4. filtrationfiltered
  5. customchromatographed on silica gel with 9:1 to 8:2 hexane

Sources & evidence

ORD record
ord-2a846899eb76410098f234781abe39dc
Source dataset
uspto-grants-1996_10
Patent number
US05569674

Linked notes

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