HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258889Generated: October 26, 2026
Potassium Iodide → Octyl p-(2-thenoyl)hydratropate
https://huagongshe.com/reaction/258889
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Suprofen | HCID 5359 | — |
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | Octyl p-(2-thenoyl)hydratropate | HCID 12232954 | — |
Reaction Steps
To a stirred mixture of 5.2 parts of p-(2-thenoyl)hydratropic acid in 50 parts of dry hexamethylphosphoramide are added 0.86 parts of sodium hydride dispersion 55.3% and the whole is stirred for 1.5 hours. Then there are added 3.86 parts of octyl bromide and 0.01 parts of potassium iodide. Upon completion, stirring is continued for 18 hours at room temperature. The reaction mixture is poured onto benzene and the whole is shaken successively twice with water, twice with sodium hydroxide solution and again twice with water. The organic phase is dried, filtered and evaporated. The residue is taken up in ether and stirred with activated charcoal. The latter is filtered off and the filtrate is evaporated again. The residue is purified by column-chromatography with chloroform. The pure fractions are collected and the solvent is evaporated, yielding octyl p-(2-thenoyl)hydratropate as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04035376 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-353a4af598504256a63ec6136961e3c1 |
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| Source note | uspto-grants-1977_07 |
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