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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047432Generated: October 26, 2026

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

https://huagongshe.com/reaction/2047432

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—
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 1/10 amount 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. Once the initiation was occurred, the rest of 3,4-dichlorobromobenzene/diethyl ether solution was added slowly with cooling to maintain the reaction temperature at 35-40° C. When everything was added, and the mixture was stirred at 40° C. for 1 hr, then cooled to 0° C. To the reaction mixture was added copper iodide(I) (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 further 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 solution was washed with aqueous ammonium chloride solution and saturated 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 numberUS08592454B2
Source datasetuspto-grants-2013_11
ORD IDord-c6da8e71da744a49810663f6d53966f6
Source noteuspto-grants-2013_11