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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676248Generated: October 30, 2026

Diethylamine → (But-3-yn-1-yl)diethylamine

https://huagongshe.com/reaction/1676248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
Reactant1,4-DioxaneHCID 31275—
Reactant3-Butynyl p-toluenesulfonateHCID 272020—
SolventDiethyl EtherHCID 3283—
Product(But-3-yn-1-yl)diethylamineHCID 1222517664.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Prepared using methodology described by Olomucki, M., et al. Ann. Chim. 1960, 5, 845. A stirred mixture of but-3-ynyl 4-methylbenzenesulfonate (21.2 g, 94.5 mmol), diethylamine (6.91 g, 94.5 mmol), and p-dioxane (100 mL) was heated to 80° C. under N2 for 6 hours. After cooling to room temperature, the suspension was diluted with diethyl ether (100 mL) and filtered. The solids were washed with diethyl ether (50 mL). The filtrate was concentrated to a brown oil. The crude was co-distilled (55-65° C.) with p-dioxane under a mild vacuum (10-50 torr). The product was obtained as an oil (7.6 g, 27%), in a 42:58 mixture with p-dioxane based on 1H NMR. 1H NMR (400 MHz, CDCl3) δ 2.70 (t, J=8 Hz, 2H), 2.55 (q, J=7 Hz, 4H), 2.32 (m, 2H), 1.97 (t, J=3 Hz, 1H), 1.04 (t, J=7 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003662B2
Source datasetuspto-grants-2011_08
ORD IDord-e7e01d8557fe42f98d105387d4d3a2b4
Source noteuspto-grants-2011_08