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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037748Generated: November 1, 2026

2-Ethyl-4-methoxy-3-methylbenzoic acid → N'-(2-(3,5-Difluorophenyl)-2-hydroxyacetyl)-2-ethyl-4-methoxy-3-methylbenzohydrazide

https://huagongshe.com/reaction/1037748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethyl-4-methoxy-3-methylbenzoic acidHCID 58298857—
Reactant3,5-DifluorophenylhydroxyacetohydrazideHCID 69809490—
ReactantHCID 178418300HCID 178418300—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN'-(2-(3,5-Difluorophenyl)-2-hydroxyacetyl)-2-ethyl-4-methoxy-3-methylbenzohydrazideHCID 6981031165%

Reaction Steps

106.0 g of 3,5-difluorophenylhydroxyacetohydrazide (B2) are dissolved in 820 ml of N,N-dimethylformamide. 104.9 g of 2-ethyl-4-methoxy-3-methylbenzoic acid (B1), 153.9 g of N-3-dimethylaminopropyl-N′-ethylcarbodiimide hydrochloride (DAPECI) and 42.8 g of hydroxybenzotriazole (HOBt) are subsequently added. The reaction mixture is cooled in an ice bath during the addition of the compounds enumerated above. The solution is then stirred at room temperature for 24 hours. For work-up, the reaction mixture is diluted with 3.5 litres of water. The resultant suspension is stirred for one hour, subsequently filtered off and washed with additional water. The filter cake is recrystallised from 2.5 litres of methanol, giving 129.0 g of the title compound as colourless solid having a melting point of 197.1° C. (MS: 401 (MNa+)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546613B2
Source datasetuspto-grants-2013_10
ORD IDord-2893ba4bf35b47d3ba99463d91e245cc
Source noteuspto-grants-2013_10