تفاعل #65196
ord-71320257f16b4873a998fad0d7a02c00
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةthe mixture is heated
- 2درجة الحرارةto reflux for 30 min
- 3استخلاصextracted three times
- 4غسيلThe combined organic phases are washed with saturated sodium chloride solution
- 5تجفيفdried over sodium sulphate
- 6تركيزAfter concentration in vacuo
- 7درجة الحرارةheated
- 8درجة الحرارةto reflux for 90 min
- 9درجة الحرارةAfter cooling to room temperature
- 10أخرىthe phases are separated
- 11غسيلthe organic phase is washed with saturated sodium chloride solution
- 12تجفيفdried over sodium sulphate
- 13تركيزconcentrated in vacuo
- 14workup.DISSOLUTIONThe residue is dissolved in methylene chloride
- 15ترشيحfiltered through silica gel
الإجراء التجريبي
804 (3.1 mmol) of diethyl 2-(cyclohexylamino)-vinyl-phosphate dissolved in 6 ml of dry tetrahydrofuran are added dropwise under nitrogen to a suspension of 59 mg (2.5 mmol) of sodium hydride in 6 ml of dry tetrahydrofuran at -5° C. After 30 min, 0.65 g (2.05 mmol) of the compound from Example 9 in 15 ml of dry tetrahydrofuran is added dropwise at the same temperature and the mixture is heated to reflux for 30 min. After cooling to room temperature, the mixture is added to 200 ml of ice-cold water and extracted three times using 100 ml of ethyl acetate each time. The combined organic phases are washed with saturated sodium chloride solution and dried over sodium sulphate. After concentration in vacuo, the residue is taken up in 5 ml of toluene, treated with a solution of 0.9 g (7 mmol) of oxalic acid dihydrate in 12 ml of water and heated to reflux for 90 min. After cooling to room temperature, the phases are separated, and the organic phase is washed with saturated sodium chloride solution, dried over sodium sulphate and concentrated in vacuo. The residue is dissolved in methylene chloride and filtered through silica gel.