HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905352Generated: October 26, 2026
Sulfuric Acid → 6-Isopropyl-2-methyl-3-cyclohexene-1-carboxylic acid
https://huagongshe.com/reaction/1905352
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Penta-1,3-diene | HCID 15301 | — |
| Reactant | 4-Methyl-pent-2-enoic acid | HCID 112103 | — |
| Reactant | 3-Isopropyl acrylic acid | HCID 642039 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-Isopropyl-2-methyl-3-cyclohexene-1-carboxylic acid | HCID 20035412 | 65.7% |
Reaction Steps
A mixture of 70 g (0.61 mol) of trans-4-methyl-2-pentenoic acid and 49 g (0.72 mol) of 1,3-pentadiene was heated for 12 hours at approx. 200° C. in an autoclave. After the reaction mixture had cooled, it was checked by means of GLC for the presence of 4-methyl-2-pentenoic acid. A further 25 g (0.36 mol) of 1,3-pentadiene were added, after which the mixture was again heated for 12 hours at 200° C. This procedure was repeated until no further decrease in the content of 4-methyl-2-pentenoic acid was any longer observed. The reaction mixture obtained was dissolved in 300 ml of ether and extracted with 300 ml of 10% NaOH solution. The alkaline solution thus obtained was acidified with 40 g of concentrated sulphuric acid and then extracted three times with ether. The ether extract was washed with water, dried on MgSO4, evaporated down and distilled. 73 g of 6-isopropyl-2-methyl-3-cyclohexene-1-carboxylic acid were obtained, b.p.: 95°-100° C./70 Pa.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04843061 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-34827857b5414388885e7bf4867918d7 |
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| Source note | uspto-grants-1989_06 |
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