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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887388Generated: October 31, 2026

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

https://huagongshe.com/reaction/887388

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. Chromatograph 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 numberUS08247418B2
Source datasetuspto-grants-2012_08
ORD IDord-e8b2d395ee024efda41b4cda0d9cbfbb
Source noteuspto-grants-2012_08