HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485409Generated: October 28, 2026
Hydrochloric Acid → HCID 13151845, compound
https://huagongshe.com/reaction/485409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Mercaptobenzoic Acid | HCID 5443 | — |
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 1,3-Dibromobenzene | HCID 7927 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13151845 | HCID 13151845 | — |
Reaction Steps
A mixture consisting of 179 g. m-dibromobenzene (0.758 mole); 46.6 g. thiosalicyclic acid (0.303 mole); 25.9 g cuprous oxide (0.181 mole); 212 cc. quinoline; and 24 cc. pyridine is mechanically stirred and heated in an oil bath at 200° C. to 210° C. for three hours. The internal temperature remains constant at 145° C. The reaction mixture is then poured into 1500 cc. of 5N aqueous HCl. The oily solid is filtered, then dissolved in 750 cc. 1N aqueous NaOH solution; this solution is filtered through celite, then extracted three times with ether. The aqueous fraction is acidified with concentrated HCl and the resulting grayish solid filtered, washed well with water and dried. The crude yield obtained is 65 g. (69.4%). It is used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536507 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-b01ca5702dc34bb2a08ef513f4716e29 |
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| Source note | uspto-grants-1985_08 |
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