HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477983Generated: November 2, 2026
Acetic Acid → tert-butyl 5-(benzylamino)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate
https://huagongshe.com/reaction/1477983
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl 5-oxohexahydrocyclopenta(c)pyrrole-2(1H)-carboxylate | HCID 10998690 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl 5-(benzylamino)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate | HCID 69225608 | 55.3% |
Reaction Steps
To a solution of tert-butyl 5-oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate (9.57 g, 42.5 mmol) in DCM (170 mL) were added BnNH2 (4.56 g, 42.5 mmol) and AcOH (2.55 g, 42.5 mmol) at 0° C. and the reaction mixture was stirred at 0° C. for 0.5 h. Then NaBH(OAc)3 (18.00 g, 85.0 mmol) was added to the above mixture and the resulting mixture was stirred at rt for another 20 h, then quenched with saturated NaHCO3 solution (142 mL), and extracted with DCM (250 mL×3). The combined organic phases were washed with brine (250 mL×3), dried over anhydrous Na2SO4, concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc) to give the title compound as a yellow solid (7.44 g, 55.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403801B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-ddcb9a4f0cdb4c9b8cf56bef73eaa338 |
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| Source note | uspto-grants-2016_08 |
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