HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846671Generated: October 31, 2026
Potassium Iodide → 7-hexyloxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3(2H)-one
https://huagongshe.com/reaction/846671
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | 7-hydroxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3(2H)-one | HCID 15724969 | — |
| Product | 7-hexyloxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3(2H)-one | HCID 15724970 | 93% |
Reaction Steps
To a solution of 7-hydroxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3(2H)-one (2.86 g), n-hexyl bromide (1.76 g) and a small amount of potassium iodide, and the mixture was heated and refluxed for 33 hours. The reaction mixture was allowed to cool. Then insoluble matter was filtered. The solvent was evaporated off under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, and was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (diluting solvent: n-hexane/ethyl acetate=9:1) to give 3.4 g (yield: 93%) of 7-hexyloxy-2-methyl-2-phenylthiazolo[3,2-a]indol-3-(2H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05137909 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-33607370258d4c6eaa76f09e5f211e59 |
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| Source note | uspto-grants-1992_08 |
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