Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420932Generated: November 1, 2026

5-Amino-4-fluoro-2-methylphenyl Methoxyformate → (4-Fluoro-5-hydroxy-2-methylphenyl) methyl carbonate

https://huagongshe.com/reaction/1420932

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-4-fluoro-2-methylphenyl MethoxyformateHCID 22625046—
ReactantSodium NitriteHCID 23668193—
CatalystCopper oxideHCID 14829—
CatalystCopper(II) nitrate trihydrateHCID 9837674—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product(4-Fluoro-5-hydroxy-2-methylphenyl) methyl carbonateHCID 2262503153.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium nitrite (1.63 g, 23 mmol) in water (19 ml) and ice (48 g) was added dropwsie to a solution of 2-fluoro-5-methoxycarbonyloxy-4-methylaniline (3.93 g, 20 mmol) in 35% sulphuric acid (48 ml) at 0° C. The reaction mixture was stirred at 0° C. for 30 minutes and a solution of copper(II)nitrate trihydrate (467 g, 1.93 mol) in water (780 ml) followed by copper(II)oxide (2.65 g, 18 mmol) were added. The solution was extracted with ethyl acetate, the organic layer was washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with petroleum ether/ethyl acetate (8/2) to give 2-fluoro-5-methoxycarbonyloxy-4-methylphenol (2.13 g, 53%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071921
Source datasetuspto-grants-2000_06
ORD IDord-0d84db538bb84c0f88fe6927961dc4ca
Source noteuspto-grants-2000_06