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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547962Generated: October 30, 2026

4-Bromotoluene → Benzothiazole,4-(4-methylphenyl)-

https://huagongshe.com/reaction/547962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromotolueneHCID 7805—
Reactant4-ChlorobenzothiazoleHCID 10821026—
CatalystPalladiumHCID 23938—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductBenzothiazole,4-(4-methylphenyl)-HCID 5429741991%

Reaction Steps

a 500 mL 2-neck round-bottomed flask was equipped with a reflux condenser and replaced by nitrogen. 70 mL of THF that was dried with 0.11 mol of Mg metal was added to the above flask and then, 0.10 mol of 1-bromo-4-methylbenzene was added in a dropwise fashion. The reaction was significantly exodermic and thus a cooling bath was equipped to reduce the temperature inside the reactor less than 50° C. It was agitated for 2 hours at room temperature, 0.11 mol of zinc chloride was added with 100 mL of THF, and further agitated for 2 hours to obtain a slurry-phase reaction mixture. Another flask was replaced by nitrogen and then 0.10 mol of 4-chlorobenzothiazole derivative, 0.10 mol of Pd, and Pd(PPh3)4 (3 mol %) were dissolved in 100 mL of THF. The prepared solution was added to the reaction mixture and then agitated 60° C. for 24 hours. After the reaction is complete, the resulting product was placed on a silica gel column to remove an inorganic slurry, and then a THF solution was concentrated under vacuum to obtain 4-para-tolylbenzo[d]thiazole using column chromatography at a yield of 91%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939669B2
Source datasetuspto-grants-2011_05
ORD IDord-ae18ed682e0d41da8a162e9bfb7a8777
Source noteuspto-grants-2011_05