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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712157Generated: October 29, 2026

Ammonia → 7-Bromobenzothiazole-2,5-diamine

https://huagongshe.com/reaction/712157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant(2-Bromo-4,6-dinitro-phenyl) thiocyanateHCID 86663954—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product7-Bromobenzothiazole-2,5-diamineHCID 8666395593.2%

Reaction Steps

To a stirred mixture of EtOH (8.37 L) and water (8.37 L) at rt was added (2-bromo-4,6-dinitro-phenyl)thiocyanate (549 g, 1.81 mol) followed by addition of Fe powder (2.02 kg, 36.11 mol) and drop wise addition of HCl (12N, 527 mL) over 30 min. The resulting reaction mixture was stirred at rt for 20 min then heated to 80° C. for 45 min. After completion of the reaction (by TLC) the reaction mixture was cooled to rt and basified to pH 8-10 by addition of aqueous ammonia solution. The resulting solution was passed through celite bed, washed with EtOAc and the combined filtrate evaporated under reduced pressure. To the resulting residue was added water (8 L) then extracted with EtOAc (2×4 L). The combined organics were washed with brine, dried (anhydrous Na2SO4), filtered and concentrated under reduced pressure to obtain the desired product (412 g, 93%). 1H NMR (DMSO-d6): δ 5.16 (br s, 2H), 6.50 (d, J=2.0 Hz, 1H), 6.53 (d, J=1.60 Hz, 1H) and 7.44 (br s, 2H). LCMS: 243.86 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181234B2
Source datasetuspto-grants-2015_11
ORD IDord-034913bfae864cb7a8656612de3c51c9
Source noteuspto-grants-2015_11