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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169961Generated: October 29, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 67081945, compound

https://huagongshe.com/reaction/1169961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant2',3'-DimethylacetophenoneHCID 16505—
Reactant1-(diethoxymethyl)-1H-imidazoleHCID 3849535—
ReactantButyllithiumHCID 178418339—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductHCID 67081945HCID 6708194576.1%

Reaction Conditions

Temperature-40 °C

Reaction Steps

1-(Diethoxymethyl)imidazole (76.0 g, 446 mmol) and N,N,N,N-tetramethylethylene diamine (67.6 mL, 446 mmol) were dissolved in 2-methyltetrahydrofuran (400 ml) and cooled to −40° C., under nitrogen. n-Butyl lithium (2.5M in hexane, 180 ml, 446 mmol) was added slowly maintaining the reaction temperature at <−25° C. throughout. The reaction mixture was stirred for an hour and allowed to warm to 0° C., after which 2,3-dimethylacetophenone (44.00 g, 297.00 mmol) was added whilst maintaining the reaction temperature at <15° C. throughout. The reaction was stirred at room temperature overnight and then quenched with aqueous hydrochloric acid (2N, 1 l). The mixture was extracted with ethyl acetate (500 ml) and to the aqueous layer was added sodium carbonate. The aqueous layer was further extracted with ethyl acetate (800 ml) and the combined extracts were washed with water (500 ml), dried (MgSO4) and concentrated in vacuo to give the title compound (48.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825149B2
Source datasetuspto-grants-2010_11
ORD IDord-ccaeb6e84c914d33be60646594be2fb6
Source noteuspto-grants-2010_11