Thionyl Chloride → HCID 86596721, compound
Reaction equation
[ClH:1].[NH2:2][CH2:3][CH2:4][C@H:5](O)[C:6]([O:8][CH3:9])=[O:7].S(Cl)([Cl:13])=O>>[ClH:13].[NH2:2][CH2:3][CH2:4][C@@H:5]([Cl:1])[C:6]([O:8][CH3:9])=[O:7]Participants
3
Procedure
To methyl (S)-4-amino-2-hydroxybutyrate hydrochloride (521.6 mg; 409.5 mg when calculated as methyl (S)-4-amino-2-hydroxybutyrate) was added 1.8 mL of thionyl chloride. The mixture was stirred at room temperature for 3 hours and then at 50° C. for 4 hours. Thereafter, the solvent was distilled off under reduced pressure to give 576.2 mg of methyl (R)-4-amino-2-chlorobutyrate hydrochloride (yield quantitative, optical purity 96.9% ee). The analysis of the optical purity was carried out by derivatizing into (R)-3-chloro-2-pyrrolidinone with sodium hydrogen carbonate, followed by high performance liquid chromatography using a chiral column (Chiralcel OB-H (Daicel)).
Workup
- waitat 50° C. for 4 hours
- distillationThereafter, the solvent was distilled off under reduced pressure
Sources & evidence
- ORD record
- ord-2fbc30a569db420ebee64a27e0dc9863
- Source dataset
- uspto-grants-2005_01
- Patent number
- US06838567B1
Reaction notes
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