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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279283Generated: October 30, 2026

1-Chloro-4-(chloromethyl)benzene → HCID 2838484, compound

https://huagongshe.com/reaction/279283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl nipecotateHCID 98969—
SolventAcetonitrileHCID 6342—
ProductHCID 2838484HCID 283848498.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

4-Chlorobenzyl chloride (6.42 g, 39.9 mmol) and iPr2NEt (7.74 g, 40.0 mmol) were added to a solution of ethyl nipecotate (6.29 g, 40.0 mmol) in CH3CN (15 mL). The reaction mixture was stirred at 70° C. for 1.5 h. The solvent was removed under reduced pressure. Saturated aqueous NaHCO (50 mL) was added to the residue and the mixture was extracted with EtOAc (100 mL). The organic phase was washed with saturated aqueous NaHCO3 and brine, and dried over Na2SO4. The solvent was removed under reduced pressure to afford ethyl 1-(4-chlorobenzyl)nipecotate as a red yellow oil (11.025 g, 97.8%) used without further purification. The purity was determined by RPLC/MS (97%); ESI/MS m/e 382.2 (M++H, C15H23ClNO2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362177B1
Source datasetuspto-grants-2002_03
ORD IDord-4c4c25d3feb94b35a25fec54be341d8a
Source noteuspto-grants-2002_03