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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930409Generated: October 30, 2026

Ethanol → Ethyl 2-(4-fluoro-2-methyl-5-nitrophenyl)acetate

https://huagongshe.com/reaction/1930409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant2-(4-Fluoro-2-methyl-5-nitrophenyl)acetic acidHCID 69038178—
ProductEthyl 2-(4-fluoro-2-methyl-5-nitrophenyl)acetateHCID 6898346181%

Reaction Conditions

Temperature85 °C

Reaction Steps

2-(4-Fluoro-2-methyl-5-nitrophenyl)acetic acid (18.43 g, 86.5 mmol, 1.00 eq) and cone. H2SO4 (4.00 ml) were combined in EtOH (300 ml) and stirred with heating at 85° C. After 2.5 h, the completed reaction was cooled to RT and concentrated as completely as possible. The residue was dissolved in MTBE (250 ml) and washed with H2O (2×) and brine (2×), dried (MgSO4), filtered and evaporated to afford ethyl 2-(4-fluoro-2-methyl-5-nitrophenyl)acetate (16.79 g, 81% yield) as a dark orange oil which was used as is in the next reaction. MS (ESI) m/z: 242.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188113B2
Source datasetuspto-grants-2012_05
ORD IDord-560f69e008cd4b729a628cdbad354b63
Source noteuspto-grants-2012_05