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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732238Generated: November 1, 2026

Sodium Dithionite → HCID 12546818, compound

https://huagongshe.com/reaction/1732238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactant1-(4-Butoxy-2,6-dimethylphenyl)-2-phenyldiazeneHCID 53762311—
SolventEthanolHCID 702—
ProductHCID 12546818HCID 12546818—

Reaction Steps

To a flask fitted with reflux condenser and stirrer containing 4-butoxy-2,6-dimethylazobenzene (53.4 g, 0.189 mole) was added 50% aqueous ethanol (480 ml). The mixture was heated close to boiling with stirring and sodium hydrosulfite (Na2S2O4, 121.4 g., 697 mole) was added in small portions over a period of 30 min. The mixture was refluxed for 75 min. Most of the alcohol was distilled off and the oily amine layer formed in the operation was taken up in ether. The aqueous phase was made alkaline with sodium hydroxide and was extracted with ether. All the combined ether extracts were dried (Na2SO4), were filtered, and all low-boiling components were evaporated at reduced pressure (solvent and aniline), after which the residue was fractionated by distillation in vacuo. The fraction boiling at 105°-108° (0.1 mm Hg) was collected. Yield: (63%); nD25 =1.5337. [Cf. E. Honkanen, Ann. Acad. Sci. Fennicae, Ser. AII, 99 (1960)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237068
Source datasetuspto-grants-1980_12
ORD IDord-77269a6c51fe437d9e979bfe8c85637c
Source noteuspto-grants-1980_12