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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421519Generated: November 3, 2026

Hydrochloric Acid → 6-Methoxybenzothiazole

https://huagongshe.com/reaction/2421519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzothiazoleHCID 7222—
ReactantTert-Butyl nitriteHCID 10906—
Reactant2-Amino-6-methoxybenzothiazoleHCID 15630—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product6-MethoxybenzothiazoleHCID 35018625.5%

Reaction Steps

2-Amino-6-methoxybenzothiazole (9.0 g) in dry DMF (10 ml) was added dropwise over 35 minutes to a stirred solution of t-butyl nitrite (9.9 ml) in DMF (40 ml) at 65° C. The temperature of the mixture was kept <73° C. during the addition. On complete addition of the solution of benzothiazole, the dark red solution was stirred for an additional 15 minutes, cooled to ambient temperature then poured into dilute hydrochloric acid (200 ml) and diluted with brine. The dark red suspension was extracted with diethyl ether and the solid filtered then washed with further water and diethyl ether. The diethyl ether extracts were combined and the aqueous fraction re-extracted with ethyl acetate. The organic fractions were combined, washed with water and dried over magnesium sulphate then evaporated to give a brown solid. The solid was purified by flash column chromatography on silica gel (40-60 mesh) eluting with hexane/ethyl acetate (4:1 by volume) to give 6-methoxybenzothiazole as a colourless solid (2.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956188B2
Source datasetuspto-grants-2011_06
ORD IDord-e643c78613d24342b71b03095488ad58
Source noteuspto-grants-2011_06