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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427820Generated: October 25, 2026

Acetic Anhydride → 1-Amino-2-naphthalenethiol

https://huagongshe.com/reaction/2427820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1-Amino-2-naphtholHCID 14535—
ReactantSodium Lauryl SulfateHCID 3423265—
SolventWaterHCID 962—
Product1-Amino-2-naphthalenethiolHCID 11331473%

Reaction Steps

5 mmol of 1-aminonaphthalene-2-ol was added to 20 mL of water, and 20 mg of sodium dodecylsulfate was added while agitating to obtain a uniform mixture. 7.5 mmol of acetic anhydride was added for 5 minutes. An acetylated product was precipitated in in 5-10 minutes. The precipitation product was filtrated and rinsed with 1 ml of water twice followed by drying under vacuum. A non-precipitated reaction mixture was extracted with 25 ml of ethyl acetate twice. The separated organic layer was dried with anhydrous sodium sulfate, and a solvent was removed using a rotatary evaporator under a reduced pressure to obtain 1-aminonaphthalene-2-thiol at a yield of 73%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968715B2
Source datasetuspto-grants-2011_06
ORD IDord-67cb42ab285f47feaa19e3083698696a
Source noteuspto-grants-2011_06