HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385009Generated: November 1, 2026
Hydrochloric Acid → 3-(3,5-Dichloro-4-hydroxybenzoyl)-1-oxo-2,3-dihydro-1,3-benzothiazole
https://huagongshe.com/reaction/385009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 3-(3,5-Dichloro-4-methoxybenzoyl)-1-oxo-2,3-dihydro-1,3-benzothiazole | HCID 68108336 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(3,5-Dichloro-4-hydroxybenzoyl)-1-oxo-2,3-dihydro-1,3-benzothiazole | HCID 51349054 | 68.2% |
Reaction Steps
3-(3,5-dichloro-4-methoxybenzoyl)-1-oxo-2,3-dihydro-1,3-benzothiazole (336 mg) was dissolved in N,N-dimethylformamide (6 mL) and lithium chloride (400 mg) was added to the solution, and then the mixture was stirred at 120° C. for 16 hours. To the reaction solution, 1N hydrochloric acid was added, and then the reaction mixture was extracted with ethyl acetate. The organic layer was washed with 1N hydrochloric acid and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was crystallized from ethyl acetate-methanol to obtain the title compound (220 mg) as a brown crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367843B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-35c30e470233476f9d37fbd68f9aaa0f |
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| Source note | uspto-grants-2013_02 |
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