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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732243Generated: October 30, 2026

Sodium Dithionite → HCID 12546817, compound

https://huagongshe.com/reaction/1732243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactant2,6-Dimethyl-4-propoxyazobenzeneHCID 54521389—
SolventWaterHCID 962—
ProductHCID 12546817HCID 12546817—

Reaction Steps

The yield of 2,6-dimethyl-4-propoxyazobenzene (20.2 g) from the previous step was dissolved in 95% alcohol (175 ml). Water was added (160 ml) and the mixture was heated to reflux. Sodium hydrosulfite (Na2S2O4) (44.8 g) was added to the boiling solution in small portions. After completion of this addition, reflux was continued for 30-60 min. The alcohol was removed by distillation at reduced pressure. The remaining heterogeneous residue was made alkaline and was extracted with ether. The ether extract was dried (Na2SO4), filtered, and evaporated. The residual oil was fractionated by distillation in vacuo. After a forerun of aniline, the desired product distilled at 101° C. (0.7 mmHg); nD25 =1.5393. The yield of 2,6-dimethyl-4-propoxyaniline was 6.86 g (51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237068
Source datasetuspto-grants-1980_12
ORD IDord-c8ac544384634b6390e1fbc60ff92ad9
Source noteuspto-grants-1980_12