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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254478Generated: November 3, 2026

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

https://huagongshe.com/reaction/1254478

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 numberUS08455488B2
Source datasetuspto-grants-2013_06
ORD IDord-f59565c1a97f488ea910b7b603e45449
Source noteuspto-grants-2013_06