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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 393614Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/393614

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Amino-4-fluoro-2-methylphenyl MethoxyformateHCID 22625046—
EduktSodium NitriteHCID 23668193—
KatalysatorCopper oxideHCID 14829—
KatalysatorCopper(II) nitrate trihydrateHCID 9837674—
LösungsmittelWaterHCID 962—
LösungsmittelSulfuric AcidHCID 1118—
Produkt(4-Fluoro-5-hydroxy-2-methylphenyl) methyl carbonateHCID 2262503153,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06809097B1
Quelldatensatzuspto-grants-2004_10
ORD IDord-35fce86474504acf894dc7bb42ac50b5
Quellennotizuspto-grants-2004_10