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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454497Generated: October 29, 2026

Dimethylformamide → Methyl 2-(benzyloxy)-5-(piperidin-1-yl)benzoate

https://huagongshe.com/reaction/454497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1,5-DibromopentaneHCID 8100—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-amino-2-(benzyloxy)benzoateHCID 23019162—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(benzyloxy)-5-(piperidin-1-yl)benzoateHCID 66990377—

Reaction Conditions

Temperature70 °C

Reaction Steps

Potassium carbonate (5.1 g) and 1,5-dibromopentane (2.5 mL) were sequentially added to an N,N-dimethylformamide (23 mL) solution of methyl 5-amino-2-(benzyloxy)benzoate (4.6 g), followed by stirring at 50 to 55° C. for 1 hour, at 55 to 60° C. for 1 hour, at 70° C. for 1 hour and 30 minutes, and then at 75 to 80° C. for 1 hour and 30 minutes. The reaction mixture was cooled to room temperature, and then water and ethyl acetate were added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [Kanto Chemical Co., Inc., silica gel 60 (spherical), eluent: 95-65% hexane/ethyl acetate] to obtain 4.3 g of methyl 2-(benzyloxy)-5-(piperidin-1-yl)benzoate as a light yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-d97f99c18f2d4c69acbacdede2703939
Source noteuspto-grants-2013_07