HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597810Generated: November 1, 2026
Sodium hydride → N-[4-(Benzothiazol-2-ylmethylthio)phenyl]acetamide
https://huagongshe.com/reaction/1597810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4'-Mercaptoacetanilide | HCID 70777 | — |
| Reactant | 2-(Bromomethyl)-1,3-benzothiazole | HCID 2776258 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[4-(Benzothiazol-2-ylmethylthio)phenyl]acetamide | HCID 8114907 | 81.2% |
Reaction Steps
79.7 mg of sodium hydride (as a 60% w/w dispersion in mineral oil) were added to a solution of 303.1 mg of 4-acetamidothiophenol in 6 ml of dimethylformamide at room temperature, followed by the addition of a solution of 454.8 mg of 2-bromomethyl-benzothiazole in 1 ml of dimethylformamide. The resulting mixture was stirred at room temperature for 2 hours, after which the reaction mixture was diluted with ethyl acetate, washed with water and then dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure and the resulting residue was purified by column chromatography through silica gel using a 1:2 by volume mixture of hexane and ethyl acetate as the eluent, to give 462.7 mg (yield 81%) of the title compound as a solid having a melting point of 147° to 149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05736487 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-e43ff76f29be45ffb85686949e392401 |
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| Source note | uspto-grants-1998_04 |
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