Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808502Generated: October 25, 2026

Nitric Acid → Benzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate

https://huagongshe.com/reaction/1808502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantBenzyl 3-(benzyloxy)-4-methoxybenzoateHCID 22070447—
SolventAcetic AnhydrideHCID 7918—
ProductBenzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoateHCID 5936200093%

Reaction Steps

To a solution of benzyl 3-(benzyloxy)-4-methoxybenzoate (6.32 g, 18.1 mmol) in Ac2O (62 mL) cooled to −10° C. under an atmosphere of N2 was added fuming HNO3 (1.5 mL, 37.1 mmol) in one portion. Stirring was continued at −10° C. for 10 minutes, then at RT for 3 hours. The reaction mixture was carefully poured into ice-water and the pH adjusted to ca. pH=5 with 5N NaOH, sat. NaHCO3 and 0.5 NaOH. The mixture was extracted with CH2Cl2 (3×200 mL). The combined organics were dried (Na2SO4), filtered and concentrated in vacuo. The residue was azeotroped with heptane to give benzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate as red colored oil (6.55 g, 16.7 mmol, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357693B2
Source datasetuspto-grants-2013_01
ORD IDord-ebec98ad6694422eb5de10408c0727bf
Source noteuspto-grants-2013_01