HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408864Generated: November 4, 2026
Methyl 5-(benzyloxycarbonylamino)bicyclo[3.2.1]octane-1-carboxylate → Methyl 5-aminobicyclo[3.2.1]octane-1-carboxylate
https://huagongshe.com/reaction/1408864
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 5-(benzyloxycarbonylamino)bicyclo[3.2.1]octane-1-carboxylate | HCID 68048076 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5-aminobicyclo[3.2.1]octane-1-carboxylate | HCID 68048077 | 51.6% |
Reaction Steps
To a solution of methyl 5-(benzyloxycarbonylamino)bicyclo-[3.2.1]octane-1-carboxylate (10 g) in methanol (150 mL) was added 10% Pd/C (1 g) and the reaction mixture was stirred under H2 (1 atm) at room temperature overnight. The reaction mixture was filtered through a Celite pad, and the filtrate was concentrated. The residue was treated with aqueous HCl (2N, 200 mL) at 0° C. and then extracted with ethyl acetate (3×100 mL) to remove organic impurities. The aqueous phase was adjusted to pH 9-10 with Sat. Na2CO3 and extracted with dichloromethane/methanol (10/1, 3×100 mL). The combined organic layer was washed with water (100 mL) and brine (100 mL), dried over sodium sulfate and concentrated under reduced pressure to afford 2.98 g of methyl 5-aminobicyclo[3.2.1]octane-1-carboxylate as a yellow oil. ESI-MS m/z: 184 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921370B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-2e030e6775aa487897c6083bdf80c0cd |
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| Source note | uspto-grants-2014_12 |
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