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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354736Generated: October 30, 2026

1,3,6-Naphthalenetrisulfonic acid → Naphthalene

https://huagongshe.com/reaction/354736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,6-Naphthalenetrisulfonic acidHCID 4438—
SolventSulfuric AcidHCID 1118—
ProductNaphthaleneHCID 931—

Reaction Steps

If a mixture containing naphthalene-1,3,6-trisulphonic acid, dissolved in sulphuric acid, such as is obtained from the trisulphonation of naphthalene, is employed, then, for example when using a naphthalenetrisulphonic acid solution in about 100% strength sulphuric acid, containing about 33.8% of naphthalene-1,3,6-trisulphonic acid, about 5.8% of naphthalene-1,3,7-trisulphonic acid and about 3.7% of naphthalene-1,3,5-trisulphonic acid, about 96% of theory of nitro-T-acid, about 3% of theory of 1-nitronaphthalene-2,5,7-trisulphonic acid and about 0.5% of theory of 2-nitronaphthalene-3,6,8-trisulphonic acid was obtained as the nitration products of the naphthalene-1,3,6-trisulphonic acid. In that case, about 45% of theory of 1-nitronaphthalene-3,5,7-trisulphonic acid and about 7% of theory of 2-nitronaphthalene-3,5,7-trisulphonic acid are additionally obtained as nitration products of the naphthalene-1,3,7-trisulphonic acid, of which latter compound about 31% of theory remains un-nitrated. Furthermore, about 62% of theory of 1-nitronaphthalene-4,6,8-trisulphonic acid and about 8% of theory of 2-nitronaphthalene-4,6,8-trisulphonic acid are obtained as nitration products of naphthalene-1,3,5-trisulphonic acid, of which latter compound about 19% of theory remains un-nitrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377535
Source datasetuspto-grants-1983_03
ORD IDord-511134e75a574245b2b0259fb9d29d36
Source noteuspto-grants-1983_03