Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963175Generated: October 29, 2026

Methyl chloroformate → Dimethyl 2-(4-chloro-2-fluorophenyl)piperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/1963175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 2-(4-chloro-2-fluorophenyl)piperidine-4-carboxylateHCID 66732030—
SolventDichloromethaneHCID 6344—
ProductDimethyl 2-(4-chloro-2-fluorophenyl)piperidine-1,4-dicarboxylateHCID 6673480186%

Reaction Steps

Methyl 2-(4-chloro-2-fluorophenyl)piperidine-4-carboxylate (7.45 g, 27.42 mmol) was dissolved into DCM (120 mL) then DIPEA (11.97 mL, 68.55 mmol) was added. Methyl carbonochloridate (3.02 mL, 38.39 mmol) was added dropwise to the solution. The mixture was stirred at room temperature for 3 h. The mixture was washed with 0.1 M HCl (2×100 mL) and satd NaHCO3 (100 mL), then dried through a phase-separator and evaporated leaving dimethyl 2-(4-chloro-2-fluorophenyl)piperidine-1,4-dicarboxylate (7.77 g, 86%) as an orange oil. MS m/z 330 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-7f64395cd86c47628f4d4fc74ffd8a09
Source noteuspto-grants-2013_04