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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224336Generated: October 30, 2026

8-(3-Nitro-p-toluenesulfonamido)-1,3,5-naphthalene trisulfonic acid trisodium salt → 8-(3-Amino-p-toluenesulfonamido)-1,3,5-naphthalenetrisulfonic acid

https://huagongshe.com/reaction/224336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-(3-Nitro-p-toluenesulfonamido)-1,3,5-naphthalene trisulfonic acid trisodium saltHCID 131711509—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
Product8-(3-Amino-p-toluenesulfonamido)-1,3,5-naphthalenetrisulfonic acidHCID 8673654867.5%

Reaction Steps

A mixture of 8.0 g of 8-(3-nitro-p-toluenesulfonamido)-1,3,5-naphthalene trisulfonic acid trisodium salt, 160 ml of water and 800 mg of 10% palladium on carbon catalyst is hydrogenated on a Parr shaker until no additional hydrogen is absorbed. The resulting mixture is filtered through diatomaceous earth and the filtrate is evaporated. The residue is dissolved in hot water and filtered. The filtrate is triturated with ethanol until cloudiness persists, then is allowed to stand at room temperature for 16 hours. The mixture is filtered and the filtrate evaporated to afford a gummy material which is dissolved in a small amount of water and triturated with ethanol. An additional 200 ml of ethanol is added and the mixture is stirred for one hour to provide a solid. The solid is collected and washed with ethanol and ether to yield 4.6 g of 8-(3-amino-p-toluenesulfonamido)-1,3,5-naphthalenetrisulfonic acid, trisodium salt as a light tan powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04231958
Source datasetuspto-grants-1980_11
ORD IDord-7ef51d4ebd2d4ee6b3676910d3819fd9
Source noteuspto-grants-1980_11