HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507702Generated: October 30, 2026
Triethylamine → 3-Ethoxy-2-hexyl-4,4-dimethylcyclobut-2-en-1-one
https://huagongshe.com/reaction/507702
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | 1-ethoxy-1-octyne | HCID 10877345 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Ethoxy-2-hexyl-4,4-dimethylcyclobut-2-en-1-one | HCID 21919563 | 61% |
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 (22 ml) was added dropwise at room temperature to a well-stirred solution of isobutyryl chloride (7.3 ml, 69 mmol) and 1-ethoxy-1-octyne [prepared according to the method of Kocienski, P. et al Tetrahedron Lett. 1833, 30, (1989)] (6.5 g, 63 mmol) in diethylether (100 ml). The reaction was warmed to 35° and stirred for 96 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 (8.6 g, 38 mmol, 61%). δH (CDCl3, 300K) 4.34 (2H, d, J 7.1 Hz), 2.05 (2H, dd, J 5.6 Hz, 7.3 Hz), 1.44 (3H, t, J 7.1 Hz), 1.27-1.12 (8H, m), 1.23 (6H, s), 0.89 (3H, t, J 2.7 Hz). m/z (ES+, 70 V) 225.0 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786177B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-77a01122d7a04403b861d4377557ddbc |
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| Source note | uspto-grants-2010_08 |
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