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Isopropanol → 1-Bromo-5-isopropoxy-2-methyl-4-nitrobenzene

HRID 1897662
Notes
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Reaction equation

HRID 1897662 reaction equation
[Br:1][C:2]1[CH:7]=[C:6](F)[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][C:3]=1[CH3:12].C(=O)([O-])[O-].[Cs+].[Cs+].[CH3:19][CH:20]([OH:22])[CH3:21]>>[Br:1][C:2]1[CH:7]=[C:6]([O:22][CH:20]([CH3:21])[CH3:19])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][C:3]=1[CH3:12]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 3776IsopropanolHCID 10796Cesium carbonateHCID 534032861-Bromo-5-fluoro-2-methyl-4-nitrobenzene

Product 1

HCID 671555871-Bromo-5-isopropoxy-2-methyl-4-nitrobenzene

Conditions

Temperature
50 °C

Procedure

To a solution of 1-bromo-5-fluoro-2-methyl-4-nitrobenzene (Step 1, 1.5 g, 6.4 mmol) in 2-propanol (30 mL) was added cesium carbonate (5.3 g, 16 mmol). The mixture was heated at 50° C. overnight. The mixture was concentrated and partitioned between ethyl acetate and water. The organic layer was concentrated and the residue was purified with silica gel column chromatography with 5% ethyl acetate in hexanes to afford 1-bromo-5-isopropoxy-2-methyl-4-nitrobenzene as a yellow solid.

Workup

  1. concentrationThe mixture was concentrated
  2. custompartitioned between ethyl acetate and water
  3. concentrationThe organic layer was concentrated
  4. customthe residue was purified with silica gel column chromatography with 5% ethyl acetate in hexanes

Sources & evidence

ORD record
ord-5eb66d1a3a484a2ca7d2dce9bc4c5cfd
Source dataset
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08519129B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes