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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl bicyclo[3.3.1]nonane-1,5-dicarboxylate | HCID 21674782 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(Methoxycarbonyl)bicyclo[3.3.1]nonane-1-carboxylic acid | HCID 727225 | 67% |
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
| 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-8d6323aaf58642598ff88c32ae62ade8 |
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| Source note | uspto-grants-2014_12 |
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