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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410167Generated: October 29, 2026

4-Aminophenol → 4-(Benzo[d]thiazol-2-ylamino)phenol

https://huagongshe.com/reaction/410167

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
Reactant2-ChlorobenzothiazoleHCID 11987—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-(Benzo[d]thiazol-2-ylamino)phenolHCID 59326813—

Reaction Steps

The solution of 2-chlorobenzothiazole (2.47 mL, 20 mmol) and 4-aminophenol (2.18 g, 20.0 mmol) in N-methylpyrrolidone (16 mL) was heated at 160° C. for 7 h. The reaction mixture was quenched with aqueous 2N NaOH and then extracted with EtOAc. The organic layer was washed with 2N NaOH. To the combined aqueous layer was added aqueous 5N HCl until pH 6, then the product was extracted with EtOAc (2×), dried (Na2SO4) and concentrated. The crude product was dissolved in MeOH and treated with SiO2. Chromatography through a Redi-Sep® pre-packed silica gel column (120 g), eluting with a gradient of 0% to 50% EtOAc in hexane, provided 4-(benzo[d]thiazol-2-ylamino)phenol as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759532B2
Source datasetuspto-grants-2014_06
ORD IDord-1c45d22c4b0445029def4bcc2baffcb6
Source noteuspto-grants-2014_06