Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344231Generated: October 30, 2026

Hydrochloric Acid → HCID 2237132, compound

https://huagongshe.com/reaction/344231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantSodium borohydrideHCID 4311764—
Reactant(3S)-5-Oxo-1-[(1S)-1-phenylethyl]-3-pyrrolidinecarboxamideHCID 54306395—
SolventTetrahydrofuranHCID 8028—
ProductHCID 2237132HCID 223713272%

Reaction Steps

(3S)-1-((S)-1-Phenylethyl)-5-oxo-3-pyrrolidinecarboxamide (150 g) was dissolved in tetrahydrofuran (2.5 l), and sodium borohydride (138 g) was added with stirring. Conc. sulfuric acid (130 ml) was dropwise added under ice-cooling. The mixture was stirred for 1 hr at room temperature, and further at refluxing temperature for 10 hr. 6N Hydrochloric acid (300 ml) was dropwise added under ice-cooling, and the mixture was stirred at refluxing temperature for 4 hr. The solvent was evaporated under reduced pressure, a 3N sodium hydroxide solution was added to make same alkaline, and the mixture was extracted with chloroform. The extract was dried over magnesium sulfate, concentrated under reduced pressure and distilled under reduced pressure to give 95 g of (3R)-3-aminomethyl-1-((S)-1-phenylethyl)pyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-f84f0933de48498183236ebbe4e1402b
Source noteuspto-grants-1999_01