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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716805Generated: November 2, 2026

Sodium Nitrite → HCID 25017231, compound

https://huagongshe.com/reaction/1716805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium NitriteHCID 23668193—
ReactantHCID 44541741HCID 44541741—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 25017231HCID 25017231109.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 1-[3-(4-methoxyphenyl)propyl]-5-[(4-methoxy)-phenyl]-2-imidazolidinone (0.6 g, 1.75 mmol) in acetic acid (15 mL) is added dropwise a solution of NaNO2 (0.12 g, 1.8 mmol) in water (1 mL). The mixture is cooled in an ice bath to 5° C. and zinc dust (0.6 g, 9 mmol) is added in portions (starting with 0.5 g addition) over 50 minutes at less than 12° C. The reaction is stirred for 5 minutes and the ice bath is removed. The reaction temperature rises quickly to about 20° C. and the reaction is maintained below about 32° C. with an ice bath. The reaction is stirred for 70 minutes at 20° C. to 27° C. and any unreacted zinc is removed by filtration. The volume of the filtrate is reduced in vacuo then diluted with dichloromethane (15 mL). To the stirred mixture is added concentrated ammonium hydroxide (2 mL), keeping the temperature below about 32° C. with an ice bath. The organic phase is separated, washed with brine, dried (Na2SO4), and concentrated to afford 0.68 g (quantitative yield) of the desired compound as a colorless oil which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803827B2
Source datasetuspto-grants-2010_09
ORD IDord-218933067b7f47f684e86d7289d8edc0
Source noteuspto-grants-2010_09