HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435073Generated: October 30, 2026
Isopropyl iodide → HCID 20490770, compound
https://huagongshe.com/reaction/435073
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | Quinoline, 1,2,3,4-tetrahydro-2,7-dimethyl- | HCID 20428348 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20490770 | HCID 20490770 | 57.6% |
Reaction Steps
A mixture of 2,7-dimethyl-1,2,3,4-tetrahydroquinoline (32.2 g, 0.2 m), potassium carbonate (15.0 g, 0.11 m), and 2-iodopropane (51 g, 0.3 m) was heated at 90°-95° C. for 5.5 hr. Progress of the reaction was slow. An additional quantity (34.0 g) of iodopropane was added and the mixture refluxed for 24 hrs. longer. Starting material was still evident by thin-layer chromatography. The reaction mixture was drowned into 200 ml water and extracted with chloroform (50 ml). The organic layer was treated with 10 ml of acetic anhydride for 1 hr. at 90°-95° C. to convert the 2,7-dimethyl-1,2,3,4-tetrahydroquinoline into N-acetyl-2,7-dimethyl-1,2,3,4-tetrahydroquinoline, which enables the recovery of the pure product by distillation. The organic layer was distilled under vacuum to give 23.4 g (55% yield) of product which boiled at 85° C. at 0.21.1 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04400318 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-93fe7a038fd24d68955619ae95095969 |
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| Source note | uspto-grants-1983_08 |
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