HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418267Generated: October 27, 2026
3-Chlorobenzohydrazide → HCID 178465636, compound
https://huagongshe.com/reaction/418267
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chlorobenzohydrazide | HCID 74289 | — |
| Reactant | HCID 178467425 | HCID 178467425 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178465636 | HCID 178465636 | — |
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
| 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-77b67856e6fb446786445493eba86381 |
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| Source note | uspto-grants-2012_01 |
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