HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262524Generated: November 3, 2026
Semicarbazide hydrochloride → HCID 53851367, compound
https://huagongshe.com/reaction/262524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Semicarbazide hydrochloride | HCID 11236 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 20195518 | HCID 20195518 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53851367 | HCID 53851367 | — |
Reaction Steps
To a mixture of 2.1 g. (0.0079 mole) of 2-nitro-3-phenylbenzofuran-7-carboxaldehyde in 70 ml. of ethanol is added 1.34 g. (0.012 mole) of semicarbazide hydrochloride and 1.07 g. (0.013 mole) of sodium acetate. The mixture is heated to its reflux temperature and maintained at reflux for 3 hours. The precipitated product is separated by filtration, washed with water and diethyl ether. The solid is washed with hot dichloroethane, separated by filtration, then dissolved in a mixture of 650 ml. of chloroform and 100 ml. of acetone by heating. This solution is washed twice with water, once with sodium bicarbonate solution, again with water, once with dilute hydrochloric acid, and twice with water. The solution is dried and the dry solution is evaporated to provide solid 2-nitro-3-phenylbenzofuran-7-carboxaldehyde semicarbazone, m.p. 249° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04154847 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-e3546252d9ba455fb2398389153bec44 |
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| Source note | uspto-grants-1979_05 |
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