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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963319Generated: October 31, 2026

Methyl chloroformate → Dimethyl 2-(3,5-difluorobenzyl)piperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/1963319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 2-(3,5-difluorobenzyl)piperidine-4-carboxylateHCID 66731630—
SolventDichloromethaneHCID 6344—
ProductDimethyl 2-(3,5-difluorobenzyl)piperidine-1,4-dicarboxylateHCID 6673495899.3%

Reaction Steps

Methyl 2-(3,5-difluorobenzyl)piperidine-4-carboxylate (7.082 g, 26.30 mmol) was dissolved in DCM (170 mL) and DIPEA (5.50 mL, 31.56 mmol), then methyl carbonochloridate (2.88 mL, 36.58 mmol) was added. The reaction mixture was stirred at room temperature for 3 h, then additional methyl carbonochloridate (0.7 mL, 8.89 mmol) was added. The solution was stirred for 30 min then washed with 0.1 M HCl and satd NaHCO3. The organic phase was dried and concentrated to give dimethyl 2-(3,5-difluorobenzyl)piperidine-1,4-dicarboxylate (8.55 g, 99%). MS m/z 328 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-611e5d7d47c54d4c9cd864a83a2e034e
Source noteuspto-grants-2013_04