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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637347Generated: October 26, 2026

Ethyl Acetate → 7-Bromo-5-nitrobenzothiazole

https://huagongshe.com/reaction/1637347

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 numberUS06040451
Source datasetuspto-grants-2000_03
ORD IDord-9e8652dbd9a94347bfbad99579f2e764
Source noteuspto-grants-2000_03