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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718880Generated: October 30, 2026

Benzyl isocyanate → Ethyl 2-(1-allyl-2-(benzylcarbamoyl)hydrazinyl)acetate

https://huagongshe.com/reaction/718880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl isocyanateHCID 76639—
ReactantEthyl (1-allylhydrazino)acetateHCID 45082254—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(1-allyl-2-(benzylcarbamoyl)hydrazinyl)acetateHCID 5954146175%

Reaction Steps

To the solution of ethyl 2-(1-allylhydrazinyl)acetate (Compound XV-1) 6.9 g (44 mmol) in tetrahydrofuran 40 ml, benzyl isocyanate 6.1 g (46 mmol) was added at 0° C. and at room temperature for 3.5 hours. The reaction mixture was diluted with ethyl acetate 150 ml and washed with water 75 ml and brine 75 ml. The organic phase was dried with magnesium sulfate and filtered. The filtrate was concentrated in vacuo to obtain the title compound 9.43 g (75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193734B2
Source datasetuspto-grants-2015_11
ORD IDord-07efee049aa44daeb5f0b224566d5de1
Source noteuspto-grants-2015_11