HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491547Generated: October 26, 2026
Triethylamine → 3-Ethoxy-4,4-dipropyl-2-cyclobuten-1-one
https://huagongshe.com/reaction/491547
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ether, ethyl ethynyl | HCID 61239 | — |
| Reactant | 2-Propylvaleryl chloride | HCID 76240 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Ethoxy-4,4-dipropyl-2-cyclobuten-1-one | HCID 21919731 | 67% |
Reaction Steps
The title compound was prepared using a modification of the method of Wasserman, H. H. et al, [J. Org. Chem, 38, 1451-1455, (1973)]; triethylamine (29 ml) was added dropwise at room temperature to a well-stirred solution of di-n-propylacetyl chloride (13.9 g, 85.8 mmol) and ethyl ethynylether (15 g, 40% solution in hexanes, 85.7 mmol) in toluene (120 ml. The reaction was warmed to 60° and stirred for 48 h prior to cooling and filtration. The filtrate was concentrated in vacuo and the residual oil chromatographed (SiO2; hexanes 80: EtOAc 20) to give the title compound as a brown oil (11.2 g, 57.1 mmol, 67%). δH (CDCl3, 300K) 5.02 (1H, s), 4.32 (2H, q, J 7.1 Hz), 1.69-1.61 (4H, m), 1.45-1.40 (4H, m), 1.02 (6H, t, J 7.3 Hz). m/z (ES+, 70V) 197.1 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531549B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-598bf1c0812f4b51ad6bbc53c5652cce |
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| Source note | uspto-grants-2009_05 |
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