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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408861Generated: November 2, 2026

Sodium Hydroxide → 5-(((Benzyloxy)carbonyl)amino)bicyclo[3.2.1]octane-1-carboxylic acid

https://huagongshe.com/reaction/1408861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 5-(benzyloxycarbonylamino)bicyclo[3.2.1]octane-1-carboxylateHCID 68048076—
SolventMethanolHCID 887—
Product5-(((Benzyloxy)carbonyl)amino)bicyclo[3.2.1]octane-1-carboxylic acidHCID 6798105649%

Reaction Steps

To a solution of methyl 5-(benzyloxycarbonylamino)bicyclo-[3.2.1]octane-1-carboxylate (25 g, crude product) in methanol (200 mL) was added NaOH (5N, 50 mL) and the reaction mixture was refluxed for two hours. After cooled to room temperature, the mixture was concentrated under reduced pressure. The residue was diluted with water (100 mL) and extracted with diethyl ether (3×100 mL) to remove the organic impurities. The aqueous phase was adjusted to pH 1˜2 with 2N aq. HCl, and extracted with dichloromethane (3×100 mL). The combined organic layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure to afford 8.5 g (49%, steps 5 and 6) of 5-(benzyloxycarbonylamino)bicyclo[3.2.1]octane-1-carboxylic acid as a yellow oil. ESI-MS m/z: 304 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921370B2
Source datasetuspto-grants-2014_12
ORD IDord-7fe8b980fe7040309dc10a5c9a6b8a0c
Source noteuspto-grants-2014_12