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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890913Generated: October 28, 2026

Ammonium thiocyanate → 1022151-32-1

https://huagongshe.com/reaction/1890913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium thiocyanateHCID 15666—
ReactantBromineHCID 24408—
Reactant4-Bromo-3-fluoroanilineHCID 821848—
SolventAcetic AcidHCID 176—
Product1022151-32-1HCID 7548096757%

Reaction Steps

To a solution of 4-bromo-3-fluoro-aniline (3.68 g, 19.37 mmol) in glacial AcOH (40 mL) was added ammonium thiocyanate (2.95 g, 38.74 mmol). When the reaction mixture was almost clear, it was placed in a cold water bath and a solution of bromine (3.1 g, 19.37 mmol) in glacial AcOH (10 mL) was added dropwise over a 10 min period. The reaction mixture was stirred at room temperature for 1 h, then it was concentrated in vacuo. The residue was partitioned between 1 N aqueous KOH and ethyl acetate. The aqueous layer was further extracted with ethyl acetate, and the combined organic layers were adsorbed on silica gel. Purification by flash chromatography on silica gel using a gradient of 0-70% ethyl acetate/hexane afforded 2.73 g of 6-bromo-5-fluoro-benzothiazol-2-ylamine as a light yellow solid (57% yield): 1H NMR (DMSO-d6) δ 7.29 (d, 1H), 7.78 (broad s, 2H), 7.99 (d, 1H); MS (m/z) 247, 249 [M+H+]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507489B2
Source datasetuspto-grants-2013_08
ORD IDord-112516d17a7f41e6a46f9ac90636a188
Source noteuspto-grants-2013_08