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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219873Generated: October 25, 2026

Carbon Dioxide → 3-(Methoxymethyl)-4-(2-methylpiperidin-1-yl)benzoic acid

https://huagongshe.com/reaction/219873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1-(4-Bromo-2-(methoxymethyl)phenyl)-2-methylpiperidineHCID 58554123—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDiethylether ethylacetateHCID 21584169—
Product3-(Methoxymethyl)-4-(2-methylpiperidin-1-yl)benzoic acidHCID 59495804—

Reaction Steps

To anhydrous Et2O (130 mL) at −78° C. was added tert-butyllithium (63.79 mL; 1.50 M; 95.68 mmol) (solution in pentane) which was followed by the slow addition of a solution of 1-[4-bromo-2-(methoxymethyl)phenyl]-2-methylpiperidine (12.97 g; 43.49 mmol) in anhydrous Et2O (20 mL). After 40 min, the reaction mixture was poured on an excess of freshly crushed dry ice and stirred for 30 min after which time it was diluted with Et2O/EtOAc (1:1, 800 mL), water (200 mL, pH 4-5). The organic layers were combined, dried over MgSO4 and the solvents were removed under reduced pressure to give a yellow oil that was triturated in iPr2O (˜20 mL) and pentane (˜20 mL), filtered off and washed with pentane to give the title compound as a beige powder. LC/MS (Method B): 264.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-936a0edee15149f29d462b20cd920a2f
Source noteuspto-grants-2012_06