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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906401Generated: October 31, 2026

Sodium Hydroxide → 2-Amino-1-naphthalenethiol

https://huagongshe.com/reaction/1906401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantNaphtho[2,1-d]thiazol-2-ylamineHCID 838513—
SolventEthylene GlycolHCID 174—
SolventWaterHCID 962—
Product2-Amino-1-naphthalenethiolHCID 12281522—

Reaction Steps

To a solution of 30.0 g sodium hydroxide in 30 mL of water and 140 mL of ethylene glycol was added 18.0 g of 2-aminobenzo[g]benzothiazole. The mixture was heated at reflux under nitrogen for 20 hours and diluted with 80 mL of water. After cooling, the mixture was filtered, then the filtrate was chilled in an ice-bath and neutralized with acetic acid. The aqueous suspension was extracted with ether (3×200 mL) and the combined extracts were dried (magnesium sulfate). Removal of the solvent gave the product to which heptane (3×150 mL) was added and the solvent was removed under reduced pressure. (This step removed traces of acetic acid). The yield of the 2-aminonaphthalene-1-thiol was 15.4 g (97%), mp 108°-110°. A sample of this compound was recrystallized from ethanol, mp 109°-110°. This compound is sensitive to air and therefore was used immediately in the next step of the synthetic scheme.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04652561
Source datasetuspto-grants-1987_03
ORD IDord-ef90eb5d59f147dca65f104d18e540d6
Source noteuspto-grants-1987_03