Triethylamine → HCID 19976954, compound

HRID 1450645Notes

Reaction equation

HRID 1450645 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-283da8893718441db20fa02db110c14b
Source dataset
uspto-grants-1997_02
Patent number
US05602160

Reaction notes

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