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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402792Generated: November 1, 2026

Nitric Acid → HCID 66759560, compound

https://huagongshe.com/reaction/1402792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantWaterHCID 962—
ReactantHCID 66758830HCID 66758830—
SolventAcetic AcidHCID 176—
ProductHCID 66759560HCID 66759560—

Reaction Conditions

Temperature30 °C

Reaction Steps

N-(4-Phenoxyphenyl)-3-(4-chlorophenyl)glutaramic acid (1.41 g) was dissolved in acetic acid (3 ml) with heating. The solution was allowed to cool to 30° C. With vigorous stirring fuming nitric acid (0.7 ml) was rapidly added in portions. The resulting hot, orange coloured solution was stirred at rt for 0.5 h. With ice cooling water (15 ml) was added slowly. From the gummy, yellow precipitate the aqueous layer is removed by decantation. Crystallisation is induced by heating with methanol (4 ml). After cooling to rt the precipitate is isolated by filtration, washed with methanol, and dried in vacuo to yield bright yellow crystals (1.21 g) of N-(2-nitro-4-phenoxyphenyl)-3-(4-chlorophenyl)glutaramic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912186B2
Source datasetuspto-grants-2014_12
ORD IDord-e47eecf253074fe2a65823fe10603515
Source noteuspto-grants-2014_12