Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951631Generated: November 4, 2026

Benzoylhydrazine → HCID 178465634, compound

https://huagongshe.com/reaction/1951631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoylhydrazineHCID 11955—
ReactantHCID 178467425HCID 178467425—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178465634HCID 178465634—

Reaction Conditions

Temperature50 °C

Reaction Steps

1-[4-((1R,2S,3R)-1,2,3,4-Tetrahydroxy-butyl)-1H-imidazol-2-yl]-ethanone (150 mg, 0.65 mmol) was suspended in methanol (3 ml) and water (1 ml). Benzoic acid hydrazide (102 mg, 0.75 mmol, 1.2 eq.) and hydrochloric acid (one drop, 12 N) were added, and the suspension was stirred at 50° C. for 18 hours. LCMS analysis indicated the formation of the product and the absence of starting material. The homogeneous reaction mixture was cooled to room temperature and concentrated in vacuo. C-18 Reverse-Phase SPE (10 g Alltech Hi-load C18, gradient from water to 20% methanol/water) to yield the product, a mixture of approximately 1:1 E:Z isomers, as a colorless solid: 193 mg (85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404732B2
Source datasetuspto-grants-2013_03
ORD IDord-11009949d97a4ce0bf1151fce38bd531
Source noteuspto-grants-2013_03