Triethylamine → HCID 19976954, compound

HRID 1440324Notes

Reaction equation

HRID 1440324 reaction equation
Cl[N:2]1[C:6](=[O:7])[CH2:5][CH2:4][C:3]1=O.[CH:9]#[C:10][CH:11](O)CC.C(N([CH2:20][CH3:21])CC)C.CC(C)=[O:24].OS(O)(=O)=O.O=[Cr](=O)=O>C(Cl)(Cl)Cl.CC(C)=O.N1C=CC=CC=1>[CH2:9]([C:3]1[CH:4]=[C:5]([C:6](=[O:7])[CH2:20][CH3:21])[O:24][N:2]=1)[CH2:10][CH3:11]

Participants

8

Procedure

Dissolved in 50 ml of chloroform were 5.0 g (57.5 mmol) of n-butylaldoxime and 0.3 ml of pyridine, to which 7.6 g (57.1 mmol) of N-chlorosuccinimide were added in small portions while the internal temperature was controlled not to exceed 35° C. After the addition, the resultant mixture was stirred at room temperature for 1 hour. To the solution, 6.0 g (71.4 mmol) of 1-pentyn-3-ol and 5.9 g (58.4 mmol) of triethylamine were added. The stirring was continued for 2 hours at 40°-50° C. After the solvent was distilled off under reduced pressure, water was added and the reaction product was then extracted with diethyl ether. After concentration, the residue was purified by silica gel chromatography (eluent: chloroform) so that 3-propyl-5-(1-hydroxypropyl)isoxazole was obtained. It was dissolved in acetone, oxidized with Jones' reagent under ice cooling, and purified by silica gel chromatography (eluent: chloroform), so that 3-propyl-5-propionylisoxazole was obtained as colorless oil.

Workup

  1. customto exceed 35° C
  2. additionAfter the addition
  3. distillationAfter the solvent was distilled off under reduced pressure, water
  4. additionwas added
  5. extractionthe reaction product was then extracted with diethyl ether
  6. concentrationAfter concentration
  7. customthe residue was purified by silica gel chromatography (eluent: chloroform) so that 3-propyl-5-(1-hydroxypropyl)isoxazole
  8. customwas obtained
  9. custompurified by silica gel chromatography (eluent: chloroform), so that 3-propyl-5-propionylisoxazole
  10. customwas obtained as colorless oil

Sources & evidence

ORD record
ord-a499386d707949d58c1ea45b3a65c68c
Source dataset
uspto-grants-1996_03
Patent number
US05498619

Reaction notes

Loading…