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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454508Generated: October 30, 2026

Potassium Iodide → Methyl 2-(benzyloxy)-5-(morpholin-4-yl)benzoate

https://huagongshe.com/reaction/454508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantBis(2-chloroethyl) etherHCID 8115—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-amino-2-(benzyloxy)benzoateHCID 23019162—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductMethyl 2-(benzyloxy)-5-(morpholin-4-yl)benzoateHCID 66990981—

Reaction Conditions

Temperature100 °C

Reaction Steps

Potassium carbonate (0.54 g), potassium iodide (0.11 g), and bis(2-chloroethyl)ether (0.22 mL) were sequentially added to an N,N-dimethylacetamide (3.2 mL) solution of methyl 5-amino-2-(benzyloxy)benzoate (0.40 g), followed by stirring at 100° C. for 3 hours. 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 [eluent: 85-60% hexane/ethyl acetate] to obtain 0.27 g of methyl 2-(benzyloxy)-5-(morpholin-4-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-85dd3bddb98b49e18ad728a192720a65
Source noteuspto-grants-2013_07