Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865793Generated: October 26, 2026

Nitric Acid → 2-Chloro-7-nitro-6-trifluoromethoxybenzothiazole

https://huagongshe.com/reaction/865793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
Reactant2-Chloro-6-(trifluoromethoxy)-1,3-benzothiazoleHCID 10037924—
SolventSulfuric AcidHCID 1118—
Product2-Chloro-7-nitro-6-trifluoromethoxybenzothiazoleHCID 10470003—

Reaction Conditions

Temperature60 °C

Reaction Steps

10 g of 2-chloro-6-trifluoromethoxybenzothiazole are added dropwise over one hour to a mixture, cooled to 10° C., of concentrated sulphuric acid (50 cm3) and concentrated nitric acid (25 cm3). The mixture is then heated for one hour at 60° C. After cooling, the mixture is poured into an ice/water mixture (1/1 by weight) and extracted with 3 times 100 cm3 of chloroform. The organic phases are dried over magnesium sulphate and concentrated under vacuum (2.7 kPa). The residue is purified by flash chromatography with a chloroform/cyclohexane mixture (4/6 by volume) as eluent. 6.4 g of 2-chloro-7-nitro-6-trifluoromethoxybenzothiazole are thus obtained, melting at 64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05567822
Source datasetuspto-grants-1996_10
ORD IDord-9e5abc2d71cc473dbcba467b15ac9a7b
Source noteuspto-grants-1996_10