HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660893Generated: October 28, 2026
4-Chlorobenzohydrazide → 2-(4-chlorobenzoyl)-N-allylhydrazinecarboxamide
https://huagongshe.com/reaction/660893
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzohydrazide | HCID 10816 | — |
| Reactant | Allyl isocyanate | HCID 15123 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-chlorobenzoyl)-N-allylhydrazinecarboxamide | HCID 49765601 | — |
Reaction Steps
Under an argon atmosphere, 19.00 g (111.4 mmol) of 4-chlorobenzoic acid hydrazide are placed in 150 ml THF. 9.44 g (111.6 mmol) of allyl isocyanate, dissolved in 110 ml THF, are added dropwise at 50° C. and the mixture further stirred overnight at 50° C. The solvent is then evaporated in vacuo, diethyl ether is added to the residue and the solid formed is isolated and purified by filtration and further washing with diethyl ether. 26.80 g (95% of theory) of the target compound are thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08084481B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-0c58f86614bb4a259ba6cadce5f07b27 |
|---|
| Source note | uspto-grants-2011_12 |
|---|