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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyryl chlorideHCID 62325—
Reactant1-ethoxy-1-octyneHCID 10877345—
SolventDiethyl EtherHCID 3283—
Product3-Ethoxy-2-hexyl-4,4-dimethylcyclobut-2-en-1-oneHCID 2191956361%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786177B2
Source datasetuspto-grants-2010_08
ORD IDord-77a01122d7a04403b861d4377557ddbc
Source noteuspto-grants-2010_08