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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hexen-2-al | HCID 12990 | — |
| Reactant | Penta-1,3-diene | HCID 15301 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(rel-(1R,2S,6S)-6-ethyl-2-methylcyclohex-3-enyl)ethan-1-one | HCID 67095432 | 516% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278230B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-04d19f0f555348bf8234241bbfe0f5b1 |
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| Source note | uspto-grants-2012_10 |
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