Reaktion #6521

ord-6cab89fbffc94bf8aa8d99d718c666ee

Reaktionsgleichung

O
water
CC(C)(C)C(=O)Cl
pivaloyl chloride
Nc1cccc(C(F)(F)F)c1
3-trifluoromethyl-aniline
CCN(CC)CC
triethylamine
CC(C)(C)C(=O)Nc1cccc(C(F)(F)F)c1
solid
Ausbeute 98.3%
CC(C)(C)C(=O)Nc1cccc(C(F)(F)F)c1
2,2-Dimethyl-3'-Trifluoromethyl-Propionanilide
Ausbeute 98.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ether (2×100 ml)
  2. 2
    WaschenThe combined ether extracts were washed successively with 0.5 HCl (100 ml)
  3. 3
    TrocknenThe ether solution was dried with MgSO4
  4. 4
    Einengenconcentrated in vacuo

Vorschrift

A solution of pivaloyl chloride (3.62 g; 30 mmol) in 40 ml dry ether was added dropwise at room temperature to a mixture of 3-trifluoromethyl-aniline (4.83 g, 30 mmol) and triethylamine (4.25 ml, 30.5 mmol). This was stirred at room temperature for a period of 14 hours and then poured into 200 ml water, extracted with ether (2×100 ml). The combined ether extracts were washed successively with 0.5 HCl (100 ml); water (2×50 ml); 7% KOH (100 ml) and water (2×50 ml). The ether solution was dried with MgSO4 and concentrated in vacuo to give a white solid (7.23 gm, 98%, m.p. 112.5° C.). The 2,2-dimethyl-3'-trifluoromethyl-propionanilide was recrystallized with dichloromethane and petroleum ether mixture.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05248781uspto-grants-1993_09