HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344231Generated: October 30, 2026
Hydrochloric Acid → HCID 2237132, compound
https://huagongshe.com/reaction/344231
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (3S)-5-Oxo-1-[(1S)-1-phenylethyl]-3-pyrrolidinecarboxamide | HCID 54306395 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 2237132 | HCID 2237132 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05864039 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-f84f0933de48498183236ebbe4e1402b |
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| Source note | uspto-grants-1999_01 |
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