HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418264Generated: October 27, 2026
Benzoylhydrazine → HCID 178465634, compound
https://huagongshe.com/reaction/418264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | HCID 178467425 | HCID 178467425 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178465634 | HCID 178465634 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093267B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-3b10e5b61eaa499f999cde4769fb8606 |
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| Source note | uspto-grants-2012_01 |
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