HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165387Generated: October 25, 2026
Water → 1,6-Dimethyl-4-(4-methyl-3-pentenyl)-3-cyclohexene-1-carboxaldehyde
https://huagongshe.com/reaction/1165387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Methyl-2-butenal | HCID 10336 | — |
| Reactant | Myrcene | HCID 31253 | — |
| Reactant | Ethyl aluminium dichloride | HCID 16686341 | — |
| Catalyst | Ethyl aluminium dichloride | HCID 16686341 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1,6-Dimethyl-4-(4-methyl-3-pentenyl)-3-cyclohexene-1-carboxaldehyde | HCID 19861574 | 44.7% |
Reaction Steps
A 3-neck reaction vessel is charged with 100 ml benzene and 50 grams of 25% ethyl aluminum dichloride in benzene. A solution containing 320 grams myrcene (85% pure), 170 grams 2-methyl-2-butenal, and 200 ml benzene is fed in at 40°-50° C. over a 1 hour period. The temperature is then raised to 60° C. and held there for 1/2 hour. An additional 10 grams ethyl aluminum dichloride solution mixed with 20 ml benzene is added and heating is continued for an additional 1/2 hour. The mixture is then cooled, water is added and the layers are separated. The organic layer is washed with water and distilled without fractionation to free the material of residue. Redistillation through an 18" Goodloe packed column provides 199 grams of 1,6-dimethyl-4-(4-methyl-3-pentenyl)-3-cyclohexene-1-carboxaldehyde (b.p. 105° C., 0.9 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04909854 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-dca29e556f0e4bae9134be75200f444a |
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| Source note | uspto-grants-1990_03 |
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