HCID 59621122, compound → HCID 59621123, compound

HRID 2061324Notes

Reaction equation

HRID 2061324 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-])=O)=[CH:4][C:3]=1[C:11]([C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=1)=O.NC1C=CC(C)=C(C(C2C=CC(OC)=CC=2)=O)C=1.NC1C=CC(C)=C(C(C2C=CC(OC)=CC=2)O)C=1>C(OCC)(=O)C.[Pd]>[NH2:8][C:5]1[CH:6]=[CH:7][C:2]([CH3:1])=[C:3]([CH2:11][C:13]2[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=2)[CH:4]=1

Participants

6

Procedure

A mixture of (2-methyl-5-nitro-phenyl)-(4-methoxy-phenyl)-methanone (5.8 g) and 10% Pd on carbon (1.0 g) in ethyl acetate (200 mL) is shaken under hydrogen atmosphere (7 bar) at ambient temperature for 4.5 h. The solution is separated from the palladium catalyst by filtration and the filtrate is concentrated in vacuo to give a mixture of the title compound, (5-amino-2-methyl-phenyl)-(4-methoxy-phenyl)-methanone and (5-amino-2-methyl-phenyl)-(4-methoxy-phenyl)-methanol. This compound mixture is dissolved in a mixture of acetonitrile (12 mL) and dichloromethane (8 mL) and the resulting solution is cooled in an ice-bath. Triethylsilane (20 mL) is added followed by the slow addition of boron trifluoride diethyl etherate (16 mL). The solution is stirred for 0.5 h at 5° C. and then quenched by the addition of aqueous sodium hydroxide solution (2 mol/L). The organic phase is separated and the aqueous phase is extracted with dichloromethane. The combined organic phases are washed with brine, dried (sodium sulphate) and concentrated in vacuo. The residue is purified by chromatography on silica gel (cyclohexane/ethyl acetate 9:1->2:1).

Workup

  1. customThe solution is separated from the palladium catalyst by filtration
  2. concentrationthe filtrate is concentrated in vacuo
  3. customto give

Sources & evidence

ORD record
ord-75b2e18ef0204b23b24a3a099e4ba996
Source dataset
uspto-grants-2012_10
Patent number
US08283326B2

Reaction notes

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