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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059555Generated: October 27, 2026

Boron trifluoride etherate → 1-(rel-(1R,2S,6S)-6-ethyl-2-methylcyclohex-3-enyl)ethan-1-one

https://huagongshe.com/reaction/2059555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantPotassium CarbonateHCID 11430—
ReactantHexen-2-alHCID 12990—
ReactantPenta-1,3-dieneHCID 15301—
SolventDichloromethaneHCID 6344—
Product1-(rel-(1R,2S,6S)-6-ethyl-2-methylcyclohex-3-enyl)ethan-1-oneHCID 67095432516%

Reaction Conditions

Temperature0 °C

Reaction Steps

At −15° C., a solution of BF3.OEt2 (54 g, 0.38 mol) in dichloromethane (680 ml) was treated within 10 min. with 3-hexen-2-one (220.1 g, 89% pure, 2 mol). 1,3-Pentadiene (490 g, 7.2 mol, precooled at 0° C.) was then added and the resulting solution stirred 30 min. at 0° C. then 1 h at 20° C. before being cooled at 0° C. and treated with a solution of 20% aqueous K2CO3 (250 ml). The resulting mixture was stirred 40 min. and concentrated (43° C. till 300 mbar). The aqueous phase was washed with hexane (500 ml) and the combined organic phases with 20% aqueous K2CO3 (100 ml), three times with saturated aqueous NaCl solution, dried (MgSO4) and concentrated. Sulzer-distillation (0.4-0.1 mbar) of the crude product (400 g) gave 1-(rel-(1R,2S,6S)-6-ethyl-2-methylcyclohex-3-enyl)ethan-1-one (326 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278230B2
Source datasetuspto-grants-2012_10
ORD IDord-04d19f0f555348bf8234241bbfe0f5b1
Source noteuspto-grants-2012_10