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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methylcyclohex-3-ene-1-carboxylic acidHCID 221278—
Reactanttert-Butyl 4-chloro-2-methylcyclohexane carboxylateHCID 546164—
Reactant3-Cyclohexene-1-carboxylic acid, 6-methyl-, (1R,6R)-rel-HCID 11309555—
ReactantHCID 14833761HCID 14833761—
ProductHCID 11208673HCID 1120867315%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06375943B1
Source datasetuspto-grants-2002_04
ORD IDord-820e86561ce14ee79a52959fbcf83850
Source noteuspto-grants-2002_04