HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280976Generated: October 30, 2026
3-Carbamoyl-1-(4-chlorobenzyl)pyrrolidin-2-one → 3-(Aminomethyl)-1-(4-chlorobenzyl)pyrrolidine
https://huagongshe.com/reaction/1280976
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Carbamoyl-1-(4-chlorobenzyl)pyrrolidin-2-one | HCID 18426256 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Aminomethyl)-1-(4-chlorobenzyl)pyrrolidine | HCID 18426251 | 66.7% |
Reaction Steps
To a solution of 3-carbamoyl-1-(4-chlorobenzyl)pyrrolidin-2-one (1.45 g) in THF (15 mL) was added 1.0 N BH3 in THF (25 mL). The reaction mixture was stirred at 65° C. for 15 h. After cooling to room temperature, the solvent was removed under reduced pressure. Water (30 mL) and conc. HCl (10 mL) were added and the mixture was stirred at 100° C. for 2 h and room temperature for 1 h. 2 N NaOH aqueous solution (100 mL) was added and the mixture was extracted with AcOEt (50 mL×3). The combined organic layers were dried over K2C3, filtered and concentrated. Column chromatography (SiO2, 15% CH3OH-5% Et3N in CH2Cl2) afforded 3-(aminomethyl)-1-(4-chlorobenzyl)pyrrolidine (860 mg, 19%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451842B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-124aa14bea874e86b0f8bb00566789ad |
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| Source note | uspto-grants-2002_09 |
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