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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963307Generated: October 29, 2026

Methyl chloroformate → Dimethyl 2-(3,4-difluorobenzyl)piperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/1963307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 2-(3,4-difluorobenzyl)piperidine-4-carboxylateHCID 66731879—
SolventDichloromethaneHCID 6344—
ProductDimethyl 2-(3,4-difluorobenzyl)piperidine-1,4-dicarboxylateHCID 6673491571.5%

Reaction Steps

Methyl 2-(3,4-difluorobenzyl)piperidine-4-carboxylate (8.115 g, 30.14 mmol) was dissolved in DCM (200 mL) and DIPEA (6.30 mL, 36.16 mmol), then methyl carbonochloridate (3.3 mL, 41.91 mmol) was added. The solution was stirred at room temperature for 2 h. The reaction mixture was washed with 0.1 M HCl satd NaHCO3. The organic phase was passed through a phase separator and evaporated. The residue was redissolved in ether/pentane, 80/20, the solution washed with 1 M HCl 5 times, then with satd NaHCO3 and brine, dried over MgSO4, filtered and evaporated to yield dimethyl 2-(3,4-difluorobenzyl)piperidine-1,4-dicarboxylate (7.05 g, 71%). MS m/z 328 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-17d9f395475a4969a20873a1d1170d17
Source noteuspto-grants-2013_04