Ethanol → 4-(Trifluoromethyl)aniline

HRID 231328Notes

Reaction equation

HRID 231328 reaction equation
C([Si](CC)(CC)O[C:5]1([C:12]([F:15])([F:14])[F:13])[CH:10]=[CH:9][C:8](=O)[CH:7]=[CH:6]1)C.Cl.[NH2:21]CC(OCC)=O.C(=O)(O)[O-].[Na+].C(O)C>O>[F:13][C:12]([F:15])([F:14])[C:5]1[CH:10]=[CH:9][C:8]([NH2:21])=[CH:7][CH:6]=1

Participants

6

Procedure

A mixture of 400 mg (1.4 mmol) of 4-triethylsiloxy-4-trifluoromethyl-2,5-cyclohexadien-1-one, 572 mg (4.2 mmol) of ethyl glycinate hydrochloride, 298 mg (3.6 mmol) of sodium bicarbonate, and 10 mL of 95% ethanol was heated to reflux for 6 hours, allowed to cool to room temperature, and poured into 25 mL of water. The resulting aqueous mixture was extracted with three 10 mL portions of dichloromethane. The organic layers were combined and extracted with six 5 mL portions of 1N HCl. Combination of the aqueous layers and treatment with solid sodium bicarbonate until neutral to pH paper gave a cloudy mixture that was extracted with three 10 mL portions of dichloromethane. The organic layers were combined, dried (MgSO4), and stripped to give a residue which was purified by PTLC (one 2 mm silica gel plate eluted with dichloromethane), affording 160 mg (73% yield) of 4-trifluoromethylaniline.

Workup

  1. temperaturewas heated
  2. temperatureto reflux for 6 hours
  3. extractionThe resulting aqueous mixture was extracted with three 10 mL portions of dichloromethane
  4. extractionextracted with six 5 mL portions of 1N HCl
  5. customgave a cloudy mixture that
  6. extractionwas extracted with three 10 mL portions of dichloromethane
  7. dry with materialdried (MgSO4)
  8. customto give a residue which
  9. customwas purified by PTLC (one 2 mm silica gel plate eluted with dichloromethane)

Sources & evidence

ORD record
ord-2a304bb2cd32477b9b1243693a04f314
Source dataset
uspto-grants-1989_07
Patent number
US04845258

Reaction notes

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