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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631373Generated: October 25, 2026

Potassium Iodide → Methyl 5-Benzyloxy-4-methoxy-2-nitrobenzoate

https://huagongshe.com/reaction/631373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-hydroxy-4-methoxy-2-nitrobenzoateHCID 53396387—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-Benzyloxy-4-methoxy-2-nitrobenzoateHCID 2266715677.1%

Reaction Conditions

Temperature92.5 °C

Reaction Steps

To solution of methyl 5-hydroxy-4-methoxy-2-nitrobenzoate (13.0 g, 0.0572 mol) in DMF (120 mL) and benzyl chloride (7.23 ml, 0.0629 mol), K2CO3 (8.69 g, 0.0629 mol) and potassium iodide (0.949 g, 0.0057 mol) were added. The reaction mixture was heated at 90-95° C. overnight. The solvent was evaporated under vacuum and the residue was taken in ethyl acetate and washed with water and brine. After drying over MgSO4, the solution was concentrated ad purified on silica gel column to yield methyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate (13.99 g, 77% yield). 1HNMR (DMSO-d6): δ 7.66 (1H, s), 7.40 (6H, m), 5.27 (2H, s), 3.83 (3H, s), 3.80 (3H, s). LC-MS (ESI) m/z 318 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09320739B2
Source datasetuspto-grants-2016_04
ORD IDord-006e04c5f87743a5919f4eeaec6a8f5b
Source noteuspto-grants-2016_04