Ammonia → 5-Oxo-pyrrolidine-3-carboxylic acid methyl ester
Reaction equation
[CH3:1][O:2][C:3](=[O:11])[C:4](=[CH2:10])[CH2:5][C:6](OC)=[O:7].[NH3:12]>CO>[O:7]=[C:6]1[NH:12][CH2:10][CH:4]([C:3]([O:2][CH3:1])=[O:11])[CH2:5]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-methylene-succinic acid dimethyl ester (158 g, 1 mol, 1 eq) in MeOH (150-160 mL) was added dropwise anhydrous liquid ammonia (17 g, 1 mol, 1 eq). The mixture was stirred at room temperature for 1.5-2 h, keeping the outlet of the flask connected with a small mercury trap (1-2 cm Hg), and left to stand overnight. Most part of MeOH was evaporated on a water bath and then residual MeOH was evaporated in vacuo until the mixture transformed into a semisolid mass. This mass was distilled in vacuo. Starting compound was distilled (bp 60-70° C. at 1 mm Hg) followed by distillation of title compound (bp 140-150° C. at 1 mm Hg) as colorless liquid, which crystallized very fast (72 g, 0.5 mol, 50%).
Workup
- customconnected with a small mercury trap
- wait(1-2 cm Hg), and left
- waitto stand overnight
- customMost part of MeOH was evaporated on a water bath
- customresidual MeOH was evaporated in vacuo until the mixture
- distillationThis mass was distilled in vacuo
- distillationStarting compound was distilled (bp 60-70° C. at 1 mm Hg)
- distillationfollowed by distillation of title compound (bp 140-150° C. at 1 mm Hg) as colorless liquid, which
- customcrystallized very fast (72 g, 0.5 mol, 50%)
Sources & evidence
- ORD record
- ord-91655aaf916649bc9a49c77e4615a642
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08357711B2
Reaction notes
Loading…