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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260906Generated: October 26, 2026

Iodine → Ethyl 3-(3,4-dichlorophenyl)-1-methylpiperidine-4-carboxylate

https://huagongshe.com/reaction/1260906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-Bromo-1,2-dichlorobenzeneHCID 29013—
ReactantEthyl 1-methyl-1,2,3,6-tetrahydro-4-pyridinecarboxylateHCID 566021—
ReactantMagnesiumHCID 5462224—
Reactant3,4-Dichlorobromobenzene diethyl etherHCID 67233472—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-(3,4-dichlorophenyl)-1-methylpiperidine-4-carboxylateHCID 6723183571.9%

Reaction Conditions

Temperature37.5 °C

Reaction Steps

To a suspension of magnesium (10.76 g) in diethyl ether (110 mL) was added a trace amount of iodine. About one-tenth of a solution of 3,4-dichlorobromobenzene (100 g) in diethyl ether (110 mL) was added slowly at 35-40° C., and the mixture was vigorously stirred until the reaction started. When the reaction started, the rest of the 3,4-dichlorobromobenzene/diethyl ether solution was added slowly while cooling the reaction mixture to 35-40° C. When all was added, the mixture was stirred at 40° C. for 1 hr, and then cooled to 0° C. To the reaction mixture was added copper(I) iodide (12.6 g), and the compound (56.2 g) obtained in step 1 was slowly added dropwise at 0° C. The reaction mixture was stirred at 0° C. for 1 hr, and at room temperature for 1 hr. The reaction mixture was poured into water (40 mL), diethyl ether (500 mL) was added, and the precipitate was removed by decantation. The reaction mixture was washed with aqueous ammonium chloride solution and brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 20% ethyl acetate/hexane→2.5% aqueous ammonia/17.5% methanol/ethyl acetate) to give crude ethyl 3-(3,4-dichlorophenyl)-1-methylpiperidine-4-carboxylate (cis/trans mixture) (75.5 g) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470816B2
Source datasetuspto-grants-2013_06
ORD IDord-02069762a3954bb8a80f7578f85e7431
Source noteuspto-grants-2013_06