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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430356Generated: November 1, 2026

Hydrochloric Acid → HCID 87132637, compound

https://huagongshe.com/reaction/1430356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-NitroanilineHCID 7475—
Reactant4-Hydroxy-2,2,6,6-tetramethylpiperidineHCID 75471—
ReactantSodium TetrafluoroborateHCID 4343483—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 87132637HCID 871326374.6%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A mixture of concentrated HCl (15 ml, 32%) and water (15 ml) is charged into 100 ml three necked round bottomed flask followed by addition of 4-nitro-aniline (5 g, 0.04 mol). The mixture is cooled to 0 to 5° C. and solution of sodium nitrite (4.14 g, 0.06 mol) in water (5 ml) is added into it while maintaining temperature 0 to 5° C. This reaction mixture is then slowly added into a solution of sodium tetrafluoroborate (6.6 g, 0.06 mol) in water (60 ml) at 0 to 5° C. The resulting solution of diazonium tetrafluoroborate salt is then added to solution of 2,2,6,6-tetramethyl-4-hydroxypiperdine (25.1 g, 0.16 mol) in acetonitrile (1000 ml)) and the mixture is stirred at 0 to −5° C. for 1 h. This reaction mixture filtered and mother liquor is evaporated to dryness at 40° C. The residue is extracted with diethyl ether (200 ml) the extract is decolorized with charcoal (50 g), filtered through bed of celite and concentrated to dryness to afford 0.56 g of 2,2,6,6-Tetramethyl-1-(4-nitrophenyldiazenyl)-piperidin-4-ol as a yellow solid, m.p. 108-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940806B2
Source datasetuspto-grants-2015_01
ORD IDord-f248639eff0c4e679ae25a27e52a7aca
Source noteuspto-grants-2015_01