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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279538Generated: October 26, 2026

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

https://huagongshe.com/reaction/279538

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 numberUS06362336B1
Source datasetuspto-grants-2002_03
ORD IDord-e70dd8e5684847159b21a5e6e481d2f3
Source noteuspto-grants-2002_03