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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249646Generated: November 1, 2026

Sodium Hydroxide → 2-Naphthol

https://huagongshe.com/reaction/1249646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium 2-naphthalenesulfonateHCID 23661868—
SolventWaterHCID 962—
Product2-NaphtholHCID 866395.3%

Reaction Steps

Sodium naphthalene-2-sulfonate and a hydrogenated triphenyl mixture were sent to a mixing tank 1 at a rate of 230 kg/hr and 825 kg/hr, respectively, and mixed with stirring. In a dispersing tank 2, 200 kg/hr of a 50% aqueous solution of sodium hydroxide was added to form a dispersed mixture. The dispersed mixture was dehydrated in a dehydrating tank 3, and sent to a reservoir 4. From the reservoir 4, a mixture consisting of sodium naphthalene-2-sulfonate, sodium hydroxide and the hydrogenated triphenyl mixture was sent to a reaction tank 5 at a rate of 1155 kg/hr, and continuously reacted at 310° C. in a nitrogen stream with a residence time of 6 hours. After the reaction, the reaction mixture was cooled in a heat exchanger 6, and sent to a water mixing tank 7 where it was mixed with 1200 liters/hr of water. Then, the reaction medium layer was separated in a separating tank 8, and the aqueous layer was mixed with 3.1 kg/hr of activated carbon in a mixing tank 9. Then, the activated carbon was removed in a filtration device 10. The residue was precipitated with dilute sulfuric acid in an acid precipitation tank 11, and separated by a centrifugal separator 12 to give 137.2 g (yield 95.3%) of 2-naphthol hourly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04633024
Source datasetuspto-grants-1986_12
ORD IDord-176c1f0e1abc4a439e9c5283ced916c2
Source noteuspto-grants-1986_12