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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759514Generated: November 2, 2026

Chloroethane → 2-Naphthol-6-sulfonic acid

https://huagongshe.com/reaction/1759514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroethaneHCID 6337—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
ReactantN-Acetyl-(1-amino-2-naphthol-6-sulfonic acid)HCID 133359—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Naphthol-6-sulfonic acidHCID 7117—
ProductN-Acetyl-(1-amino-2-naphthol-6-sulfonic acid)HCID 133359—
Product2-Naphthalenesulfonic acid, 5-amino-6-ethoxy-HCID 222166—

Reaction Steps

12.5 parts of 1-acetamino-2-hydroxy-naphthalene-6-sulphonic acid (67.5% pure=8.5 parts of 100% pure), prepared according to Example 4, and 4.2 parts of potassium carbonate are suspended in a mixture of 47.4 parts by weight of methanol and 9.0 parts by weight of water in an autoclave. After heating the autoclave, 6.2 parts of 25% strength potassium hydroxide solution and 5.8 parts of ethyl chloride are simultaneously metered in at 120° C. The reaction mixture is worked up analogously to Example 12. 87% of theory of 1-amino-2-ethoxy-naphthalene-6-sulphonic acid, relative to 1-acetamino-2-hydroxy-naphthalene-6-sulphonic acid, or 67.8% of theory, relative to 2-hydroxy-naphthalene-6-sulphonic acid, are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04341719
Source datasetuspto-grants-1982_07
ORD IDord-d9d6743fe5a84dddb35021e780b3007d
Source noteuspto-grants-1982_07