HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547962Generated: October 30, 2026
4-Bromotoluene → Benzothiazole,4-(4-methylphenyl)-
https://huagongshe.com/reaction/547962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromotoluene | HCID 7805 | — |
| Reactant | 4-Chlorobenzothiazole | HCID 10821026 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzothiazole,4-(4-methylphenyl)- | HCID 54297419 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07939669B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-ae18ed682e0d41da8a162e9bfb7a8777 |
|---|
| Source note | uspto-grants-2011_05 |
|---|