تفاعل #1483034
ord-cce2c988fe3744559e6927abad67dcee
معادلة التفاعل
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المعالجة
- 1workup.DISSOLUTIONhad dissolved
- 2أخرى(1 h)
- 3أخرىThe resulting reaction mixture
- 4درجة الحرارةwas warmed to room temperature
- 5workup.STIRRINGstirred for 2 h
- 6غسيلIt was then washed with brine
- 7تجفيفdried over Na2SO4
- 8ترشيحfiltered
- 9تركيزconcentrated under reduced pressure
- 10أخرىPurification by silica gel chromatography (CH2Cl2)
الإجراء التجريبي
In a typical run, nicotinic acid (2.0 g, 16.2 mmol) was taken up in CH2Cl2 (20 mL) along with oxalyl chloride (1.4 mL, 16.2 mmol). After a few drops of DMF were added, the reaction mixture was stirred at room temperature until all the solids had dissolved and all gas evolution had ceased (1 h). This freshly prepared solution of the acid chloride was added dropwise at 0° C. to a solution containing tert-butyl 2-aminoethylcarbamate (2.6 g, 16.2 mmol) and Et3N (3.4 mL, 24.2 mmol) in CH2Cl2 (200 mL). The resulting reaction mixture was warmed to room temperature and stirred for 2 h. It was then washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. Purification by silica gel chromatography (CH2Cl2) afforded tert-butyl 2-(nicotinamido)ethylcarbamate (3.1 g, 74%).