تفاعل #3104

معادلة التفاعل

sodium cyanoborohydride

HCl

ethyl 2-(4-methoxyphenyl)-4-(3,4-methylenedioxyphenyl)-4,5-dihydro-3H -pyrrole-3-carboxylate

→

title compound

المردود 96.8%

Ethyl 2-(4-methoxyphenyl)-4-(3,4-methylenedioxyphenyl)-pyrrolidine 3-carboxylate

المردود 96.8%

المذيبات

ethanol

ظروف التفاعل

المعالجة

1. 1
   أخرىInto a 12-L flask equipped with magnetic stirring, addition funnel, temperature probe, and nitrogen inlet
2. 2
   أخرىThe reaction vessel was degassed with nitrogen
3. 3
   workup.ADDITIONAbsolute 3.7 L ethanol and 1.12 L of THF were added
4. 4
   workup.ADDITIONwas then added
5. 5
   workup.ADDITIONafter addition
6. 6
   أخرىAfter the starting material was consumed
7. 7
   workup.ADDITION0.5 L of 7% aq. NaHCO3 was added
8. 8
   تركيزThe reaction mixture was concentrated
9. 9
   workup.ADDITIONdiluted with 5 L ethyl acetate
10. 10
    غسيلThe organic layer was washed twice with 2 L of 7% aq. NaHCO3 and once with 2.5 L of 23% aq. NaCl
11. 11
    تجفيفthe dried over 190 g MgSO4
12. 12
    ترشيحfiltered
13. 13
    تركيزconcentrated

الإجراء التجريبي

Into a 12-L flask equipped with magnetic stirring, addition funnel, temperature probe, and nitrogen inlet was charged 0.460 kg ethyl 2-(4-methoxyphenyl)-4-(3,4-methylenedioxyphenyl)-4,5-dihydro-3H -pyrrole-3-carboxylate (1.25 mol). The reaction vessel was degassed with nitrogen. Absolute 3.7 L ethanol and 1.12 L of THF were added. 31 mg bromocresol green and 94.26 g sodium cyanoborohydride (1.5 mol) were added. A solution containing 400 mL absolute ethanol and 200 mL of 12M HCl was then added. The reaction mixture was stirred for 30 minutes after addition was complete. After the starting material was consumed, 0.5 L of 7% aq. NaHCO3 was added. The reaction mixture was concentrated and diluted with 5 L ethyl acetate. The organic layer was washed twice with 2 L of 7% aq. NaHCO3 and once with 2.5 L of 23% aq. NaCl, the dried over 190 g MgSO4, filtered, and concentrated to give 447 g of the title compound as a thick yellow oil.

المصدر