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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-(4-Fluoro-2-methyl-5-nitrophenyl)acetic acid | HCID 69038178 | — |
| Product | Ethyl 2-(4-fluoro-2-methyl-5-nitrophenyl)acetate | HCID 68983461 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188113B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-560f69e008cd4b729a628cdbad354b63 |
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| Source note | uspto-grants-2012_05 |
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