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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352840Generated: November 1, 2026

Sodium Cyanide → HCID 19437357, compound

https://huagongshe.com/reaction/1352840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant(1,1'-Biphenyl)-4-carboxaldehydeHCID 76689—
ReactantAmmonium CarbonateHCID 517111—
SolventEthanolHCID 702—
ProductHCID 19437357HCID 1943735742%

Reaction Steps

A solution of 4-biphenylcarboxaldehyde (4.6 g 25 mmol), sodium cyanide (3.68 g 75 mmol) and ammonium carbonate (9.60 g 100 mmol) in 50% aqueous ethanol (175 ml) was heated at 50° C. for 20 hours. The reaction mixture was cooled, concentrated under reduced pressure and acidified to pH 2.0 with concentrated hydrochloric acid (fume hood). The intermediate 4-(4-phenylphenyl)-2,5-imidazolinedione was collected by filtration, washed with dilute (0.5%) HCl and dried before using as crude in the next stage. (Filtrates were retained and treated with sodium hypochlorite solution before disposal) The intermediate 4-(4-phenylphenyl)-2,5-imidazolinedione was refluxed in 16% aqueous sodium hydroxide (100 ml, 16% w/v) for 24 h. The reaction mixture was then filtered, cooled, diluted with water (100 ml) and then shaken with ethyl acetate and separated. The aqueous solution was adjusted to pH 5.1 with concentrated hydrochloric acid and the solid obtained collected by filtration, washed with a little water and dried to give 4-phenylphenylglycine (2.36 g, 42%). 1H nmr (d6 DMSO) consistent with desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220781B2
Source datasetuspto-grants-2007_05
ORD IDord-66300468063b4c289184f6bc1d133e91
Source noteuspto-grants-2007_05