HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597792Generated: October 30, 2026
Water → N-[4-(5-Fluorobenzothiazol-2-ylmethoxy)phenyl]butyramide
https://huagongshe.com/reaction/1597792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | 4-(5-Fluorobenzothiazol-2-ylmethoxy)aniline | HCID 18932237 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[4-(5-Fluorobenzothiazol-2-ylmethoxy)phenyl]butyramide | HCID 18932318 | 55% |
Reaction Steps
0.09 ml of triethylamine and 0.07 ml of butyryl chloride were added to a solution of 150.8 mg of 4-(5-fluorobenzothiazol-2-ylmethoxy)aniline [prepared as described in step (b) above] in 3 ml of methylene chloride cooled in an ice-water bath. The temperature of the resulting mixture was then elevated to room temperature and the mixture was stirred for 1 hour. At the end of this time, water was added to the reaction mixture and the resulting mixture was extracted with methylene chloride. The resulting extract was washed consecutively with water and a saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure and the resulting residue was recrystallized from a mixed solvent of methylene chloride and hexane to give 104.5 mg (yield 55%) of the title compound as a solid having a melting point of 201° to 202° 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-2c956fa856aa4c6fbf5fcb9c27423468 |
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| Source note | uspto-grants-1998_04 |
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