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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447570Generated: October 26, 2026

1,3,6-Naphthalenetrisulfonic acid, 8-amino-, sodium salt (1:?) → 8-(4-Nitro-2-sulfobenzamido)-1,3,6-naphthalenetrisulfonic acid tetrasodium salt

https://huagongshe.com/reaction/1447570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,6-Naphthalenetrisulfonic acid, 8-amino-, sodium salt (1:?)HCID 101899—
ReactantSodium Acetate TrihydrateHCID 23665404—
Reactant4-Nitro-2-sulfobenzoic anhydrideHCID 57002923—
SolventWaterHCID 962—
Product8-(4-Nitro-2-sulfobenzamido)-1,3,6-naphthalenetrisulfonic acid tetrasodium saltHCID 131711368—

Reaction Steps

To an ice-bath cooled solution (5° C.) of 8-amino-1,3,6-naphthalenetrisulfonic acid trisodium salt and 6.7 g of sodium acetate trihydrate in 100 ml of water is added 8.8 g of 4-nitro-2-sulfobenzoic acid anhydride. The mixture is stirred vigorously for 10 minutes and is filtered. The filtrate is cooled in an ice bath and diluted with 500 ml of cold ethyl alcohol. The mixture is filtered and the product is washed with ethyl alcohol and ether and then is dried. The product is dissolved in 50 ml of warm water and is stirred for 10 minutes after the addition of one ml of acetone. The mixture is treated with activated charcoal, filtered through diatomaceous earth and is washed with 20 ml of water. The filtrate is cooled in an ice bath and acidified with 1.5 ml of concentrated hydrochloric acid. The solution is diluted with 500 ml of cold ethyl alcohol, and the precipitated material is filtered, washed with ethanol followed by ether and dried. The above purification process is repeated without acidification. The product obtained is dried overnight at 110° C. to give 18.5 g of 8-(4-nitro-2-sulfobenzamido)-1,3,6-naphthalenetrisulfonic acid tetrasodium salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04177209
Source datasetuspto-grants-1979_12
ORD IDord-97f8776749c74c99978ac63f8e98c66a
Source noteuspto-grants-1979_12