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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10398Generated: October 30, 2026

4-Bromo-2-nitrobenzene-1-thiol → 2-amino-4-bromobenzene-1-thiol

https://huagongshe.com/reaction/10398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-nitrobenzene-1-thiolHCID 21980019—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
Product2-amino-4-bromobenzene-1-thiolHCID 12199294—

Reaction Steps

The mixture of 4-bromo-2-nitro-benzenethiol and its disulfide from Example 2A (14.9 g, 53.5 mmol) in THF (450 mL) was mixed with Raney Ni (30 g, 100% wt). The mixture was hydrogenated in a 1000 mL Paar shaker at a hydrogen pressure of 40 psi at 50° C. for 41 hours. When the reaction was complete, the solids were filtered. The solid filter-cake was dissolved in pyridine (600 mL) at 100° C. and filtered to remove the Ni residue. This pyridine solution contained mostly the 2-amino-4-bromophenyldisulfide. Crude yield=11.9 g (92%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094790B2
Source datasetuspto-grants-2006_08
ORD IDord-047fe1c5f9834cbcb16b3e4e1a1cbfb3
Source noteuspto-grants-2006_08