HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648699Generated: October 30, 2026
Potassium Iodide → HCID 14127331, compound
https://huagongshe.com/reaction/648699
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13594461 | HCID 13594461 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 14127331 | HCID 14127331 | 81.6% |
Reaction Steps
A mixture of 5.0 g of methyl 3-oxo-2,3,4,5-tetrahydro-1-benzoxepin-2-carboxylate, 7.1 g of 1-bromo-3-chloropropane, 1.5 g of potassium iodide, 6.3 g of potassium carbonate and 60 ml of acetonitrile is heated under refluxing for 4 hours. After cooling, the inorganic substances are filtered off and the filtrate is concentrated under reduced pressure. The residue is treated with water and then extracted with ethyl acetate. The organic layer is washed with water, dried, and evaporated under reduced pressure. The residue is purified by column chromatography on silica gel (eluant: hexane:ethyl acetate=8:1→2:1), to give 5.5 g of methyl 2-(3-chloropropyl)-3-oxo-2,3,4,5-tetrahydro-1-benzoxepin-2-carboxylate as a colorless oil. Recrystallization from ethanol gives 4.4 g of colorless prisms: m.p. 75°-77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04736031 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-52f1a086ab2f4622b566249a7fee8229 |
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| Source note | uspto-grants-1988_04 |
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