HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536535Generated: October 31, 2026
Diethyl Ether → 2-(4-chlorobenzoyl)-N-allylhydrazinecarboxamide
https://huagongshe.com/reaction/536535
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Chlorobenzohydrazide | HCID 10816 | — |
| Reactant | Allyl isocyanate | HCID 15123 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-chlorobenzoyl)-N-allylhydrazinecarboxamide | HCID 49765601 | — |
Reaction Steps
An amount of 5.00 g (29.3 mmol) of 4-chlorobenzenecarbohydrazide was suspended in dry tetrahydrofuran (150 ml) at 50° C. and then 2.63 ml (29.9 mmol) of allyl isocyanate in solution in 110 ml of dry tetrahydrofuran were added dropwise. The starting material underwent temporary complete dissolution, and then a fine precipitate was produced. The mixture was stirred at 50° C. for 2 hours. After cooling to room temperature it was admixed with diethyl ether. The colourless solid was isolated by suction filtration, washed with diethyl ether and dried in a high vacuum. This gave 7.42 g (100% of theory) of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859601B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-05249b8f506b45a1825876bb1d23e412 |
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| Source note | uspto-grants-2014_10 |
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