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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408859Generated: November 1, 2026

Dimethyl bicyclo[3.3.1]nonane-1,5-dicarboxylate → 5-(Methoxycarbonyl)bicyclo[3.3.1]nonane-1-carboxylic acid

https://huagongshe.com/reaction/1408859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl bicyclo[3.3.1]nonane-1,5-dicarboxylateHCID 21674782—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-(Methoxycarbonyl)bicyclo[3.3.1]nonane-1-carboxylic acidHCID 72722567%

Reaction Steps

A solution of dimethyl bicyclo[3.3.1]nonane-1,5-dicarboxylate (8.32 g, 36.8 mmol) and Ba(OH)2.8H2O (5.80 g, 18.4 mmol) in ethanol (40 mL) and H2O (10 mL) was refluxed overnight. After cooled to room temperature, the mixture was concentrated under reduced pressure. The resulting residue was added diluted with water (100 mL) and extracted with diethyl ether (3×200 mL). The combined organic layer was washed with brine (100 mL), dried over sodium sulfate and concentrated under reducer pressure to recover starting material as an orange oil. 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 (100 mL), dried over sodium sulfate and concentrated under reduced pressure to afford 1.8 g (67%) of 5-(methoxycarbonyl)bicyclo[3.3.1]nonane-1-carboxylic acid as a white solid. ESI-MS m/z: 213 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921370B2
Source datasetuspto-grants-2014_12
ORD IDord-8d6323aaf58642598ff88c32ae62ade8
Source noteuspto-grants-2014_12