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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant4-ChlorobenzohydrazideHCID 10816—
ReactantAllyl isocyanateHCID 15123—
SolventTetrahydrofuranHCID 8028—
Product2-(4-chlorobenzoyl)-N-allylhydrazinecarboxamideHCID 49765601—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859601B2
Source datasetuspto-grants-2014_10
ORD IDord-05249b8f506b45a1825876bb1d23e412
Source noteuspto-grants-2014_10