HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842436Generated: October 31, 2026
6-Methylcyclohex-3-ene-1-carboxylic acid → HCID 11208673, compound
https://huagongshe.com/reaction/842436
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Methylcyclohex-3-ene-1-carboxylic acid | HCID 221278 | — |
| Reactant | tert-Butyl 4-chloro-2-methylcyclohexane carboxylate | HCID 546164 | — |
| Reactant | 3-Cyclohexene-1-carboxylic acid, 6-methyl-, (1R,6R)-rel- | HCID 11309555 | — |
| Reactant | HCID 14833761 | HCID 14833761 | — |
| Product | HCID 11208673 | HCID 11208673 | 15% |
Reaction Steps
Test compounds: Liquid trimedlure (UOP Chemicals, East Rutherford, N.J.) (98% pure; density 1.02 g/ml) and ceralure (Agrisense/Biosys, Palo Alto, Calif.) (98% pure; density 1.43 g.ml) were purchased from commercial sources. The 2 g polymeric plug (Agrisense/Biosys, Palo Alto, Calif.) was the same product used by action agencies such as USDA-APHIS and California Department of Food and Agriculture (CDFA) in their surveillance and detection programs against medfly. The enantiomers of ceralure B1 (ethyl-cis-5-iodo-trans-2-methylcyclohexane-1-carboxylate) (henceforth referred to as the 1R,2R,5R and 1S,2S,5S enantiomers respectively) were synthesized using the 9 step process (described above) which yielded both enantiomers with high purity (97% ) and an overall yield of 15%. The racemic mixture of the two enantiomers was produced starting from racemic (5), which is (1RS, 6RS)-6-methyl-3-cyclohexene-1-carboxylic acid, using the above described process used to produce ethyl (1R,2R,5R)-5-iodo-2-methylcyclohexane-1-carboxylate (4a).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06375943B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-820e86561ce14ee79a52959fbcf83850 |
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| Source note | uspto-grants-2002_04 |
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