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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287331Generated: October 28, 2026

Benzaldehyde → HCID 19261677, compound

https://huagongshe.com/reaction/2287331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant2-ImidazolidinoneHCID 8453—
ReactantSodium NitriteHCID 23668193—
CatalystZincHCID 23994—
SolventSulfuric AcidHCID 1118—
ProductHCID 19261677HCID 1926167787%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirring solution of 65 g (0.75 mole) of 2-imidazolidinone in 2000 ml of 2 N H2SO4 is cooled to SAC. A 53 g (0.77 mole) portion of NaNO2 is added portionwise, over a 15 minute period, maintaining the temperature at 0° C. The resulting mixture is stirred at 0° C. for 2 hours. A 108 g (1.65 mole) portion of zinc dust is added portionwise, over a 1 hour period, maintaining the temperature at 0° C. The reaction is stirred at 0° C. for 0.5 hour and then at ambient temperature for 1 hour. The excess zinc is removed by filtration. The filtrate is treated all at once, with a solution of 80 g (0.75 mole) of benzaldehyde, in 400 ml of S.D.A. #32 and the resulting mixture is stirred for 16 to 18 hours at ambient temperature. The solid is collected by filtration, washed with H2O, and air-dried to yield 124 g (87%) of 1-[(phenylmethylene)amino]-2-imidazolidinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083945
Source datasetuspto-grants-2000_07
ORD IDord-bb4f1fc7dcff4a5bb4d3b3addcdbe99c
Source noteuspto-grants-2000_07