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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174922Generated: November 1, 2026

2-Chloro-6-nitrobenzothiazole → 2-Chloro-1,3-benzothiazol-6-amine

https://huagongshe.com/reaction/1174922

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-nitrobenzothiazoleHCID 75476—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Product2-Chloro-1,3-benzothiazol-6-amineHCID 1092120333.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

Suspend 2-Chloro-6-nitro-benzothiazole (21.43 g, 99.8 mmol) in glacial acetic acid (300 mL). Add elemental iron (12.9 g, 231 mmol) and stir at 40° C. for 5 h. Filter the reaction mixture through Celite®, concentrate in vacuo, and adsorb onto silica gel. Subject the residue to silica gel flash column chromatography in two portions [(120 g column, 0-10% CH3OH/CH2Cl2), (120 g column, 0-5% CH3O/CH2Cl2)] to yield the desired product (6.17 g, 33%). mass spectrum (m/e): 185.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838543B2
Source datasetuspto-grants-2010_11
ORD IDord-7a11f8b797054b5bb9358e1d3b5b4014
Source noteuspto-grants-2010_11