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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300401Generated: October 26, 2026

Ethyl Acetate → 7-Bromo-5-nitrobenzothiazole

https://huagongshe.com/reaction/2300401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantNitrosylsulfuric acidHCID 82157—
ReactantPhosphinic AcidHCID 4124402—
Reactant7-Bromo-5-nitrobenzo[d]thiazol-6-amineHCID 22728034—
SolventSulfuric AcidHCID 1118—
Product7-Bromo-5-nitrobenzothiazoleHCID 2272803189%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5-nitro-6-amino-7-bromobenzothiazole (1.0 g, 3.7 mmol) in 4 mL of sulfuric acid was added nitrososulfuric acid (1.2 g, 9.5 mmol) in a portion. The resulting reaction mixture was stirred for 12 h at 25° C. The reaction mixture was then cooled to 0° C. and 1 mL of H3PO2 was added into the solution. It was stirred for 12 h at another 25° C. and for 2 h at 50° C. The reaction mixture was then poured into EtOAc and washed with aq. NaHCO3. Organic layer was dried over Na2SO4 and concentrated in vacuo to provide an oil (0.85 g, 3.2 mmol, 89%), which was characterized as the desired product(>95% pure) and subjected to a following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498177B2
Source datasetuspto-grants-2002_12
ORD IDord-9c5c3e7259a444ffaacea8305ed79486
Source noteuspto-grants-2002_12