Hydrochloric Acid → 3-Acetamidopyrrolidine
Reaction equation
[C:1]([NH:4][CH2:5][CH:6]1[CH2:9][N:8]([CH:10](C2C=CC=CC=2)C2C=CC=CC=2)C1)(=[O:3])[CH3:2].Cl>[Pd].C(O)C>[C:1]([NH:4][CH:5]1[CH2:6][CH2:9][NH:8][CH2:10]1)(=[O:3])[CH3:2]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 12.5 g (0.057 mol) of the compound obtained in stage c) above, 1.3 g of 10% Pd/C, 80 ml of 95% ethanol and a drop of concentrated hydrochloric acid is hydrogenated at 40° C. When the theoretical quantity of hydrogen has been consumed, it is filtered and the filtrate is concentrated to obtain 6.5 g of the title compound in the form of an oily product.
Workup
- customis hydrogenated at 40° C
- customWhen the theoretical quantity of hydrogen has been consumed
- filtrationit is filtered
- concentrationthe filtrate is concentrated
Sources & evidence
- ORD record
- ord-1a928d4b37604e8baac71fe30740b07e
- Source dataset
- uspto-grants-1996_11
- Patent number
- US05576320
Reaction notes
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