N-butyl-4-chlorobenzamide → n-Butyl-4-chlorobenzenemethanamine

HRID 1533973

Reaktionsgleichung

Reaktionsgleichung von HRID 1533973
C([NH:5][C:6](=O)[C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=1)CCC.[H]1[BH2][H][BH2]1.Cl.O>C1COCC1>[CH2:6]([C:12]1[CH:11]=[C:10]([Cl:13])[CH:9]=[CH:8][C:7]=1[CH2:6][NH2:5])[CH2:7][CH2:8][CH3:9]

Komponenten

4

Versuchsvorschrift

A solution of N-butyl-4-chlorobenzamide (2.26 g; 0.011 mol) in dry THF (25 ml) was added slowly to an ice-cooled solution of 1.0M B2H6 --THF complex (45 ml; 0.045 mol) under a nitrogen blanket. When addition was complete, the mixture was stirred and heated to reflux for 3 hours, cooled and decomposed by dropwise addition of 1:1 conc aq HCl-water (10 ml). The mixture was then evaporated on a rotary evaporator at 60° for 1/2 hour to decompose the boron-amine complexes. The residue was taken up in water, strongly basified with aq NaOH and extracted with CH2Cl2 (3×25 ml). The combined extracts were washed with water, dried (MgSO4), filtered and evaporated to give n-butyl-4-chlorobenzenemethanamine (1.79 g) as an oil. The oil was converted to the hydrochloride salt of the title compound (1.98 g) by crystallising from ethanolic HCl and ethyl acetate, mp 250°-252° after melting and resolidifying at 203°-207° .

Aufarbeitung

  1. additionWhen addition
  2. temperatureheated
  3. temperatureto reflux for 3 hours
  4. temperaturecooled
  5. customThe mixture was then evaporated on a rotary evaporator at 60° for 1/2 hour
  6. extractionextracted with CH2Cl2 (3×25 ml)
  7. washThe combined extracts were washed with water
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-0798807ca7414d15b147a8763d9f2864
Quelldatensatz
uspto-grants-1992_02
Patentnummer
US05086073

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