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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060183Generated: October 31, 2026

Hydrochloric Acid → HCID 57105160, compound

https://huagongshe.com/reaction/1060183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
ReactantEthyl chloroformateHCID 10928—
Reactant4-MethoxypyridineHCID 69278—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57105160HCID 5710516044%

Reaction Steps

A mixture of 4-methoxypyridine (0.4 mol) in THF (1000 ml) was stirred and cooled in a 2-propanol/CO2 bath. Ethyl chloroformate (0.4 mol) was added dropwise and the mixture was stirred for 3 hours while cooling (mixture I). In another round-bottom flask, the Grignard-reagent was prepared: Mg (0.44 mol) was stirred in a small amount of (C2H5)2O. Some 12 was added. A small amount of 1,2-dichloro-4-(chloromethyl)-benzene was added. Then, 1,2-dichloro-4-(chloromethyl)benzene (0.4 mol) in (C2H5)2O (600 ml) was added dropwise at reflux temperature. The mixture was stirred for one hour (mixture II). The Grignard-reagent was decanted off, added to mixture I at <−40° C., and the resulting reaction mixture was stirred, allowing the temperature to reach RT. The reaction mixture was stirred for one hour at RT. HCl (10%, 800 ml) was added and the mixture was stirred for 30 minutes, then CH2Cl2 was added. The organic layer was separated, dried, filtered and the solvent evaporated, yielding 57.8 g (44%) of (±)-ethyl 6-[(3,4-dichlorophenyl)methyl]-1,2,3,4-tetrahydro-4-oxo-1-pyridinecarboxylate (intermediate 9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521621B1
Source datasetuspto-grants-2003_02
ORD IDord-c4f3e131b9fd4cc2b08415b7f011fb43
Source noteuspto-grants-2003_02