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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253602Generated: October 29, 2026

Dimethylformamide → Methyl 2-(3-((3-methoxypropoxy)(phenyl)methyl)piperidin-1-yl)acetate

https://huagongshe.com/reaction/253602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
Reactant3-((3-Methoxypropoxy)(phenyl)methyl)piperidine hydrochlorideHCID 66861971—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(3-((3-methoxypropoxy)(phenyl)methyl)piperidin-1-yl)acetateHCID 5778648227%

Reaction Steps

3-((3-Methoxypropoxy)(phenyl)methyl)piperidine HCl salt (63 mg, 0.212 mmol) was mixed with methyl bromoacetate (20 μL), K2CO3 (75 mg, 2.5 equiv.), and anhydrous DMF (3 mL). The mixture was stirred overnight at rt. LC-MS indicated the reaction was complete. The mixture was diluted with EtOAc and washed with water. The water layer was extracted with EtOAc. The combined organic layers were washed with water and brine, and dried over Na2SO4. After concentration, the residue was purified by flash chromatography on a 4-g silica gel cartridge eluted with a 0-10% methanol in dichloromethane gradient to afford methyl 2-(3-((3-methoxypropoxy)(phenyl)methyl)piperidin-1-yl)acetate (19 mg, 27% yield). LC-MS (3 min) tR=1.07 min, m/z 336 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872028B2
Source datasetuspto-grants-2011_01
ORD IDord-fb7e025a645648d28fba30e78bd34132
Source noteuspto-grants-2011_01