HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986936Generated: October 29, 2026
Water → 1-Isopropyl-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/986936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2,3,4-Tetrahydroquinoline | HCID 69460 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 1-Isopropyl-1,2,3,4-tetrahydroquinoline | HCID 15555625 | 72.1% |
Reaction Steps
In 60 ml of N,N-dimethylformamide were dissolved 13.8 g of 1,2,3,4-tetrahydroquinoline. To the resulting solution were added 21.1 g of isopropyl iodide and 20.6 g of potassium carbonate, followed by stirring under heat at 60° C. for 5 hours. Water was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue so obtained was subjected to chromatography on a silica gel column (developing solvent: 3% ethyl acetate/n-hexane), whereby 13.1 g of the title compound were obtained in the form of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06630463B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-aaadb4a0219543ea950793d67f455c72 |
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| Source note | uspto-grants-2003_10 |
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