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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992735Generated: October 31, 2026

3-Chlorobenzohydrazide → HCID 178465636, compound

https://huagongshe.com/reaction/1992735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorobenzohydrazideHCID 74289—
ReactantHCID 178467425HCID 178467425—
CatalystHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178465636HCID 178465636—

Reaction Conditions

Temperature50 °C

Reaction Steps

1-[4-((1R,2S,3R)-1,2,3,4-Tetrahydroxy-butyl)-1H-imidazol-2-yl]-ethanone (194 mg, 0.84 mmol) was suspended in ethanol (4 ml) and water (1 ml). 3-chlorobenzoic acid hydrazide (170 mg, 1.0 mmol, 1.2 eq.) and hydrochloric acid (one drop, 12 N) were added, and the suspension was stirred at 50° 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 a ˜3:1 E:Z mixture, as a white solid: 108 mg (33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649098B2
Source datasetuspto-grants-2010_01
ORD IDord-815bb5396b774d4f9ab6da3acfd2b95e
Source noteuspto-grants-2010_01