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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951635Generated: October 26, 2026

4-Fluorobenzohydrazide → HCID 178465640, compound

https://huagongshe.com/reaction/1951635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzohydrazideHCID 9972—
ReactantHCID 178467425HCID 178467425—
CatalystHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178465640HCID 178465640—

Reaction Conditions

Temperature55 °C

Reaction Steps

1-[4-((1R,2S,3R)-1,2,3,4-Tetrahydroxy-butyl)-1H-imidazol-2-yl]-ethanone (172 mg, 0.74 mmol) was suspended in ethanol (4 ml) and water (1 ml). 4-fluorobenzoic acid hydrazide (131 mg, 0.85 mmol, 1.1 eq.) and hydrochloric acid (one drop, 12 N) were added, and the suspension was stirred at 55° C. for 48 hours. LCMS analysis indicated the formation of the product and the absence of starting material. The reaction mixture was cooled to room temperature, and partially concentrated in vacuo. The resulting white precipitate was collected and washed with ethanol to yield the product, as one apparent isomer, as a white solid: 97 mg (35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404732B2
Source datasetuspto-grants-2013_03
ORD IDord-c5f69ce9b1194f5292a261aab4d27a27
Source noteuspto-grants-2013_03