تفاعل #50506
ord-196a48b2d40b41e897ee47e90e526120
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONAfter the addition
- 2درجة الحرارةthe mixture was gradually heated
- 3أخرىwhile separating water as an azeotrope
- 4درجة الحرارةrefluxed for 2 hours
- 5workup.DISTILLATIONBenzene was distilled off under reduced pressure
- 6workup.DISSOLUTIONthe residue was dissolved in ethanol (100 ml)
- 7workup.STIRRINGWith stirring at 10° to 15° C.
- 8workup.ADDITIONsodium borohydride (0.9 g) was added little by little
- 9workup.STIRRINGThe mixture was then stirred at room temperature for 2 hours
- 10workup.DISTILLATIONEthanol was distilled off at less than 30° C
- 11workup.ADDITIONDichloromethane was added to the residue
- 12أخرىa portion of it soluble in dichloromethane was separated
- 13workup.DISTILLATIONDichloromethane was distilled off under reduced pressure, and volatile materials
- 14أخرىwere removed at 1 mmHg and less than 60° C.
الإجراء التجريبي
5-Trifluoromethylpicoline aldehyde (3.5 g) was added dropwise at room temperature to a solution of trimethylenediamine (7.4 g) in benzene (70 ml). After the addition, the mixture was gradually heated with stirring, and then while separating water as an azeotrope, refluxed for 2 hours. Benzene was distilled off under reduced pressure, and then the residue was dissolved in ethanol (100 ml). With stirring at 10° to 15° C., sodium borohydride (0.9 g) was added little by little. The mixture was then stirred at room temperature for 2 hours. Ethanol was distilled off at less than 30° C. Dichloromethane was added to the residue, and a portion of it soluble in dichloromethane was separated. Dichloromethane was distilled off under reduced pressure, and volatile materials were removed at 1 mmHg and less than 60° C. to give N-(5-trifluoromethyl-2-pyridylmethyl)trimethylenediamine (3.5 g) as a colorless oil.