HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491546Generated: October 27, 2026
Triethylamine → (+/-) 3-Ethoxy-4-methyl-4-propyl-2-cyclobuten-1-one
https://huagongshe.com/reaction/491546
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ether, ethyl ethynyl | HCID 61239 | — |
| Reactant | 2-Methylvaleryl chloride | HCID 107385 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (+/-) 3-Ethoxy-4-methyl-4-propyl-2-cyclobuten-1-one | HCID 21919694 | 77% |
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)]; to a solution of 2-methyl pentanoyl chloride (3.91 ml) and ethyl ethynylether (5 g, 40% solution in hexanes, 28.6 mmol) in Et2O (35 ml) at room temperature was added triethylamine (9.9 ml), with stirring. The reaction was warmed to 50° and stirred for 72 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 colourless oil (3.71 g, 17.9 mmol, 77%). δH (CDCl3, 300K), 4.84 (1H, s), 4.24-3.98 (2H, m), 2.04 (3H, s), 1.56-1.43 (4H, m), 1.30-1.26 (3H, m), 0.91 (3H, t, J 7.3 Hz). m/z (ES+, 70V) 178.1 (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-2304bbd292924b4fb42ad0522b8ae7e5 |
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| Source note | uspto-grants-2009_05 |
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