HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285995Generated: October 30, 2026
Iodoethane → 1-Ethyl-2,2,4-trimethyl decahydroquinoline
https://huagongshe.com/reaction/2285995
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Decahydroquinoline | HCID 92911 | — |
| Reactant | 2,2,4-Trimethyldecahydroquinoline | HCID 22628786 | — |
| Product | 1-Ethyl-2,2,4-trimethyl decahydroquinoline | HCID 20543105 | — |
Reaction Steps
1-ethyl-2,2,4-trimethyl decahydroquinoline was prepared by the reaction of the intermediate saturated decahydroquinoline with the alkyl halide. 36.3 grams (0.2 mole) of 2,2,4-trimethyl decahydroquinoline of about 76% cis structure was placed into a reactor vessel equipped for heating and agitation. 15.6 grams (0.1 mole) of iodoethane was added dropwise to the reactor vessel. The mix was heated to 105° C. while stirring for 3 hours. A thick slurry formed which was filtered out and washed with acetone. The acetone wash liquid was then concentrated and distilled using a 3" Vigreaux column to yield 7.1 grams of a product boiling at 58°-60° C. at 0.25 mm Hg. The NMR spectra of the product was consistent with the desired product, 1-ethyl-2,2,4-trimethyl decahydroquinoline. Calculated carbon, hydrogen, nitrogen content for the formula C14H27N is 80.31% carbon, 13.00% hydrogen, and 6.69% nitrogen while the measured contents were 79.93% carbon, 13.54% hydrogen, and 6.35 % nitrogen respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04326061 |
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| Source dataset | uspto-grants-1982_04 |
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| ORD ID | ord-080e8c98b1c24056863e595ef5c0795b |
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| Source note | uspto-grants-1982_04 |
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