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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262499Generated: November 1, 2026

Acetyl chloride → (4-Acetylmorpholin-2-yl)methyl 4-phenylpiperazine-1-carboxylate

https://huagongshe.com/reaction/2262499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantMorpholin-2-ylmethyl 4-phenylpiperazine-1-carboxylate dihydrochloride saltHCID 66934509—
SolventPyridineHCID 1049—
Product(4-Acetylmorpholin-2-yl)methyl 4-phenylpiperazine-1-carboxylateHCID 4263435778.1%

Reaction Steps

To a stirred solution of morpholin-2-ylmethyl 4-phenylpiperazine-1-carboxylate dihydrochloride (Example 10; 0.52 g, 1.40 mmol) in pyridine (2.25 mL, 27.7 mmol) was slowly added acetyl chloride (0.15 mL, 2.10 mmol). The reaction mixture was stirred at room temperature for 1 h before the pyridine was removed in vacuo and the resulting residue diluted with sat aq NaHCO3 solution (50 mL). The organic product was extracted with EtOAc (3×50 mL). The combined organic layers were washed with sat aq NaHCO3 solution (3×50 mL), dried (MgSO4) and the solvent removed in vacuo. The residue was purified by column chromatography (normal phase, 20 g, Strata SI-1, silica gigatube, 20 mL/min, gradient 0% to 5% MeOH in EtOAc). The solvents were removed in vacuo and dried in a vacuum oven overnight to afford (4-acetylmorpholin-2-yl)methyl 4-phenylpiperazine-1-carboxylate (0.38 g, 78%) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851471B2
Source datasetuspto-grants-2010_12
ORD IDord-f05833b15f5e404cbb1803df93812b6b
Source noteuspto-grants-2010_12