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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167874Generated: November 1, 2026

1-Chloroethyl chloroformate → 2-[4-(2,6-Dichloro-phenoxymethyl)-phenyl]-morpholine

https://huagongshe.com/reaction/2167874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant4-Benzyl-2-[4-(2,6-dichloro-phenoxymethyl)-phenyl]-morpholineHCID 67032591—
Solvent1,2-DichloroethaneHCID 11—
Product2-[4-(2,6-Dichloro-phenoxymethyl)-phenyl]-morpholineHCID 6703242078.3%

Reaction Steps

To a solution of 4-benzyl-2-[4-(2,6-dichloro-phenoxymethyl)-phenyl]-morpholine (2.25 g; 3.7 mmol) in 1,2-dichloroethane (10 mL), was added dropwise 1-chloroethyl chloroformate (0.44 mL; 4.0 mmol), at 0° C. After 15 minutes, the cooling was removed and subsequently the mixture was heated under reflux overnight. After cooling to RT the mixture was concentrated in vacuo. To the residue was added toluene and the mixture was concentrated in vacuo. This last step was repeated twice. To the final residue was added MeOH (10 mL), and this mixture was stirred overnight at RT. Once more the mixture was concentrated in vacuo. The residue was partitioned between EtOAc and 2 M Aqueous NaOH. The layers were separated, and the organic layer dried (Na2SO4), filtered, and concentrated in vacuo to afford 2-[4-(2,6-Dichloro-phenoxymethyl)-phenyl]-morpholine (0.98 g), which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045441B2
Source datasetuspto-grants-2015_06
ORD IDord-0101a98ecd53429e931a094c967f873a
Source noteuspto-grants-2015_06