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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383416Generated: October 31, 2026

Ethyl Acetate → 5-Amino-4-fluoro-2-(1-methylcyclohexyl)phenyl methyl carbonate

https://huagongshe.com/reaction/383416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium formateHCID 2723923—
Reactant4-Fluoro-2-(1-methylcyclohexyl)-5-nitrophenyl methyl carbonateHCID 59395013—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5-Amino-4-fluoro-2-(1-methylcyclohexyl)phenyl methyl carbonateHCID 5135844582.1%

Reaction Steps

To a solution of 4-fluoro-2-(1-methylcyclohexyl)-5-nitrophenyl methyl carbonate 24.1 g, 77.5 mmol) in 220 mL of CH3OH was added Pd/C 10%, 9.6 g, then ammonium formate (26.7 g, 445 mmol) was portion-wise added to the above reaction mixture at room temperature until starting material is consumed. The mixture was filtrated and the filtrate was evaporated under vacuum. The residue was purified by column chromatography on silica gel diluted with hexane:ethyl acetate=50:1 to give 5-amino-4-fluoro-2-(1-methylcyclohexyl)phenyl methyl carbonate as a red brown oil (17.9 g, 82% yield). 1H NMR (400 MHz, CDCl3) δ 6.99 (d, J=13.6 Hz, 1H), 6.51 (d, J=8.4 Hz, 1H), 3.89 (s, 3H), 3.43 (brs, 2H), 1.96-1.91 (m, 2H), 1.58-1.38 (m, 8H), 1.18 (s, 3H): MS m/z: 281.9 [M+H]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367660B2
Source datasetuspto-grants-2013_02
ORD IDord-9a15bfb69ef24a55b3728b263384da67
Source noteuspto-grants-2013_02