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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507988Generated: November 4, 2026

Dimethylformamide → Methyl 4-[(4-hydroxypiperidin-1-yl)methyl]-3-isopropoxybenzoate

https://huagongshe.com/reaction/507988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantPiperidin-4-olHCID 79341—
ReactantHCID 23157338HCID 23157338—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-[(4-hydroxypiperidin-1-yl)methyl]-3-isopropoxybenzoateHCID 2315734383%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of methyl 4-(bromomethyl)-3-isopropoxybenzoate (2.0 g, 6.96 mmol), 4-hydroxypiperidine (1.06 g, 10.4 mmol), potassium carbonate (1.44 g, 10.4 mmol) and N,N-dimethylformamide (20 mL) was stirred at 70° C. for 20 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (basic silica gel, hexane/ethyl acetate=10/1-hexane/ethyl acetate=1/2) to give the title compound (1.77 g, yield 83%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-c3b48a72b5684cd680c808926deac83c
Source noteuspto-grants-2010_08