Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187798Generated: October 31, 2026

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

https://huagongshe.com/reaction/2187798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
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 1Pr2NEt (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 NaHCO3 (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, C15H21ClNO2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410566B1
Source datasetuspto-grants-2002_06
ORD IDord-5f58d7ce419f462aa64f89e3b1b419fa
Source noteuspto-grants-2002_06