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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588242Generated: October 29, 2026

1-Chloroethyl chloroformate → (2,6-Dichloro-phenyl)-(4-morpholin-2-yl-phenyl)-amine

https://huagongshe.com/reaction/588242

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant[4-(4-Benzyl-morpholin-2-yl)-phenyl]-(2,6-dichloro-phenyl)-amineHCID 66653766—
Solvent1,2-DichloroethaneHCID 11—
Product(2,6-Dichloro-phenyl)-(4-morpholin-2-yl-phenyl)-amineHCID 6665421560.5%

Reaction Steps

To a solution of [4-(4-benzyl-morpholin-2-yl)-phenyl]-(2,6-dichloro-phenyl)-amine (0.72 g; 1.74 mmol) in 1,2-dichloroethane (5 mL) was added, drop wise, ACE-Cl (0.40 mL; 3.66 mmol) at 0° C. The resulting mixture was stirred at room temperature, overnight, and subsequently 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 (5 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 (2,6-dichloro-phenyl)-(4-morpholin-2-yl-phenyl)-amine (0.34 g); which was used as such.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227960B2
Source datasetuspto-grants-2016_01
ORD IDord-c71054398c8a400c8ff91d625164c402
Source noteuspto-grants-2016_01