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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | [4-(4-Benzyl-morpholin-2-yl)-phenyl]-(2,6-dichloro-phenyl)-amine | HCID 66653766 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | (2,6-Dichloro-phenyl)-(4-morpholin-2-yl-phenyl)-amine | HCID 66654215 | 60.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227960B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-c71054398c8a400c8ff91d625164c402 |
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| Source note | uspto-grants-2016_01 |
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