Ethanol → 4-(Trifluoromethyl)aniline

HRID 1085345Notes

Reaction equation

HRID 1085345 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 dichlormethane. The organic layers were combined and extracted with six 5 mL portions of IN 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 dichlormethane
  4. extractionextracted with six 5 mL portions of IN 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-3ef59b32a68b4156aa9363a7cb252d3c
Source dataset
uspto-grants-1991_04
Patent number
US05008425

Reaction notes

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