تفاعل #44497
ord-499dc9a566d3415a9db0ac30f2538769
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1workup.ADDITIONAfter the addition
- 2workup.ADDITIONwere added
- 3درجة الحرارةThen, heating
- 4أخرىThe solvent was evaporated
- 5أخرىthe residue was partitioned with diethyl ether and water
- 6غسيلThe organic phase was washed with a NaHCO3 solution until the washes
- 7أخرىIt was then dried
- 8ترشيحfiltered
- 9أخرىevaporated
- 10أخرىThe residue was purified over silica gel using 2-30% diethyl ether in hexanes
الإجراء التجريبي
3-Bromo-2-bromomethyl-propionic acid methyl ester (30 g, 115 mmol) was added to a stirred solution of freshly distilled 1-cyclohex-1-enyl-pyrrolidine (20.4 mL, 126 mmol) and triethyl amine (35 mL, 252 mmol) in dry CH3CN (400 mL). After the addition, the mixture was heated (100° C.) and stirred for twelve hours before acetic acid (20 mL) and water (100 mL) were added. Then, heating was continued for another three hours. The solvent was evaporated and the residue was partitioned with diethyl ether and water. The organic phase was washed with a NaHCO3 solution until the washes became basic. It was then dried, filtered, and evaporated. The residue was purified over silica gel using 2-30% diethyl ether in hexanes to give the title compound as a clear oil.