HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896780Generated: October 25, 2026
Sodium Hydroxide → 2-(4-Chlorophenyl)-6-(methylthio)benzo[d]thiazole
https://huagongshe.com/reaction/1896780
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Chloro-N-(4-(methylthio)phenyl)benzothioamide | HCID 57617480 | — |
| Catalyst | Potassium ferricyanide | HCID 26250 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Chlorophenyl)-6-(methylthio)benzo[d]thiazole | HCID 57617482 | 67.2% |
Reaction Steps
To a solution of potassium hexacyanoferrate(III) (670 mg, 2.04 mmol) in water (5 mL) at 90° C. was added dropwise over 5 minutes a solution of 4-chloro-N-(4-(methylthio)phenyl)benzothioamide (150 mg, 0.51 mmol) in ethanol (2 mL) and 3M aqueous sodium hydroxide solution (1.4 mL, 4.08 mmol). The resulting mixture was heated at 90° C. for 30 minutes. After cooling, the precipitate formed was filtered off and washed with water to give a yellow solid. The yellow solid was purified by column chromatography eluting using a gradient (hexanes to ethyl acetate/hexanes 5:95 v/v) to afford 100 mg (67%) of the title compound (LCMS RT=9.37 min, MH+ 292.2)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518980B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-7c90c261aa124935b19fa2f6e63667d7 |
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| Source note | uspto-grants-2013_08 |
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