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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393614Generated: October 26, 2026

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

https://huagongshe.com/reaction/393614

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 dropwise to a solution of (5-amino-4-fluoro-2-methylphenyl) methyl carbonate (3.93 g, 20 mmol) in 35% sulphuric acid (48 ml) at 0° C. The 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) was 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 (4-fluoro-5-hydroxy-2-methylphenyl) methyl carbonate (2.13 g, 53%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809097B1
Source datasetuspto-grants-2004_10
ORD IDord-35fce86474504acf894dc7bb42ac50b5
Source noteuspto-grants-2004_10