HCID 22501934, compound → HCID 22501864, compound

HRID 1814670Notes

Reaction equation

HRID 1814670 reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[CH:11]=[CH:10][C:9]([N+:12]([O-])=O)=[C:8]([C:15]([F:18])([F:17])[F:16])[CH:7]=2)[CH2:3][CH2:2]1>C(O)C>[CH:1]1([CH2:4][O:5][C:6]2[CH:11]=[CH:10][C:9]([NH2:12])=[C:8]([C:15]([F:16])([F:17])[F:18])[CH:7]=2)[CH2:3][CH2:2]1

Participants

3

Conditions

Temperature
70 °C

Procedure

Stannous chloride (4.75 g, 21 mmol) was added to a solution of 4-cyclopropylmethoxy-1-nitro-2-trifluoromethylbenzene (1.1 g, 4.2 mmol) in ethanol (12 mL). The reaction temperature was raised to 70° C. for 1.5 hour. The reaction mixture was concentrated in vacuo and the residue dissolved in ethyl acetate (20 mL). Water (15 mL) was added and sodium hydrogen carbonate was added until pH 7. The mixture was filtered and the organic phase collected. The aqueous phase was extracted with ethyl acetate (20 mL). The combined organic phases were dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography (38 g) using heptane and ethyl acetate (9:1) as eluent to give 0.49 g of 4-cyclopropylmethoxy-2-trifluoromethylphenylamine.

Workup

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. dissolutionthe residue dissolved in ethyl acetate (20 mL)
  3. additionWater (15 mL) was added
  4. additionsodium hydrogen carbonate was added until pH 7
  5. filtrationThe mixture was filtered
  6. customthe organic phase collected
  7. extractionThe aqueous phase was extracted with ethyl acetate (20 mL)
  8. dry with materialThe combined organic phases were dried (MgSO4)
  9. concentrationconcentrated in vacuo
  10. customThe residue was purified by flash chromatography (38 g)

Sources & evidence

ORD record
ord-cc5be6ff04be4cdfab0f091cda8d88ed
Source dataset
uspto-grants-2005_04
Patent number
US06875760B2

Reaction notes

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