Ammonium Chloride → 1-(2-Bromopropanoyl)pyrrolidine
Reaction equation
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[Br:6][CH:7]([CH3:11])[C:8](Cl)=[O:9].[Cl-].[NH4+]>ClCCl>[Br:6][CH:7]([CH3:11])[C:8]([N:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1)=[O:9]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Pyrrolidine (0.12 mol, 8.3 g) was added to stirred solution of 2-bromopropanoyl chloride (0.58 mol, 10 g) in dichloromethane (200 ml) at 0° C. After 0.5 hour, the reaction mixture was warmed to room temperature, stirred for 2 hours, and saturated ammonium chloride solution (20 ml) was added. The solvent was evaporated and the mixture was extracted with ethyl acetate (200 ml). The organic phase was separated, dried over anhydrous sodium sulfate, filtered and concentrated to dryness. The residue was purified by column chromatography (silica gel, dichloromethane/methanol=55:1) to give 2-bromo-1-(pyrrolidin-1-yl)propan-1-one (9.8 g, 93%). LCMS (M+H+) m/z: calcd 205.01. found 205.
Workup
- customThe solvent was evaporated
- extractionthe mixture was extracted with ethyl acetate (200 ml)
- customThe organic phase was separated
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated to dryness
- customThe residue was purified by column chromatography (silica gel, dichloromethane/methanol=55:1)
Sources & evidence
- ORD record
- ord-cddfa12b120a4a8a9dc7e8065e747670
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09085583B2
Reaction notes
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