Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-(benzyloxycarbonylamino)bicyclo[3.2.1]octane-1-carboxylateHCID 68048076—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 5-aminobicyclo[3.2.1]octane-1-carboxylateHCID 6804807751.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921370B2
Source datasetuspto-grants-2014_12
ORD IDord-2e030e6775aa487897c6083bdf80c0cd
Source noteuspto-grants-2014_12