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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272042Generated: November 4, 2026

Toluene → HCID 18456485, compound

https://huagongshe.com/reaction/1272042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDimethyl oxalateHCID 11120—
Reactant1-(3-Fluoro-4-methoxyphenyl)ethan-1-oneHCID 96828—
ReactantPotassium t-amylateHCID 23683543—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18456485HCID 1845648584%

Reaction Steps

To a solution of 3-fluoro-4-methoxyacetophenone (2.59 g, 15.4 mmol) and dimethyl oxalate (2.0 g, 16.9 mmol) in THF (25 ml) was portionwise added a 1.7 M solution of potassium tert-amylate in toluene (25 ml, 42.5 mmol). The mixture was stirred at room temperature for 14 hours. Water (1.0 ml) and more THF (25 ml) were added, and stirring at room temperature was continued for 30 hours. Water (250 ml) was added, and the mixture was washed with a mixture of heptane and toluene. The aqueous phase was filtered, acidified with concentrated hydrochloric acid (6.0 ml), and filtered. After drying, 3.09 g (84%) of 4-(3-fluoro-4-methoxyphenyl)-4,2-dioxobutyric acid was obtained. A mixture of this acid (1.99 g, 8.29 mmol), ethanol (75 ml), and hydrazine hydrate (0.80 ml, 2 equiv.) was refluxed for 18 hours. Water (250 ml) and concentrated hydrochloric acid (4.0 ml) were added, and the mixture was filtered. After drying under reduced pressure 1.76 g (90%) of 5-(3-fluoro-4-methoxyphenyl)-2H-pyrazole-3-carboxylic acid acid was obtained as a solid. This acid was used to prepare the title amide using General Procedure (D).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208497B2
Source datasetuspto-grants-2007_04
ORD IDord-6fd29ccd9bd8442497068edda0ed5609
Source noteuspto-grants-2007_04