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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544807Generated: November 1, 2026

2-(Dimethylamino)ethanol → 3-[2-(Dimethylamino)ethoxy]-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-1-butanone

https://huagongshe.com/reaction/544807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
Reactant(E)-1-(2,6,6-trimethylcyclohex-2-en-1-yl)but-2-en-1-oneHCID 5366077—
Product3-[2-(Dimethylamino)ethoxy]-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-1-butanoneHCID 5930406832%

Reaction Steps

A solution of α-damascone (6.44 g; 33.5 mmol), N,N-dimethylaminoethanol (30.25 ml; 301 mmol) and tetramethylguanidine (TMG) (0.77 g; 6.70 mmol) was heated at 70° C. for 15 h. Afterward, the excess of N,N-dimethylaminoethanol was distilled at ca. 60° C./10 to 2 mbar. The crude product was diluted in diethyl ether (Et2O) and this mixture was extracted with 5% aqueous HCl and washed with water and saturated aqueous NaCl. The combined aqueous phases were basified using aqueous NaOH and extracted twice with ether to recover the crude product in the organic phases. The organic phases were still washed with water and brine, then dried over Na2SO4 and concentrated. Bulb-to-bulb distillation of the crude product (100-125° C./0.05 mbar) afforded 2.94 g of the desired pure product (yield: 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935669B2
Source datasetuspto-grants-2011_05
ORD IDord-fef90a884c8b410eaec07245978ae5f9
Source noteuspto-grants-2011_05