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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507682Generated: October 27, 2026

Dimethyl Sulfide → HCID 57428875, compound

https://huagongshe.com/reaction/507682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantN,N-Diethyl-para-anisamideHCID 231459—
ReactantHCID 178511841HCID 178511841—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57428875HCID 57428875—

Reaction Steps

Sec-BuLi (1.4 M in cyclohexane, 11.34 mL, 15 mmol) was carefully added to a mixture of N,N,N′,N′-tetramethylethane-1,2-diamine (2.2 mL, 15 mmol) in anhydrous THF at −78° C. N,N-Diethyl-4-methoxybenzamide (3 g, 14.4 mmol) dissolved in 5 mL of anhydrous THF was added dropwise to the reaction mixture which was allowed to stir for 1 h Dimethyl sulfide (2.5 mL, 28.8 mmol) was then added to the reaction. After stirring for 15 min, the cooling bath was removed and the mixture was stirred overnight. The reaction was diluted with ethyl acetate and washed with a solution of saturated sodium bicarbonate, water and then brine. The organic layer was then dried with sodium sulfate, concentrated and purified by flash chromatography using a gradient of 20 to 80% ethyl acetate in hexanes to obtain the product as a light yellow oil. Yield=2.51 g. MS (M+H)+ 254.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786132B2
Source datasetuspto-grants-2010_08
ORD IDord-9eaf5759cfb642039848c8751e9e1b0f
Source noteuspto-grants-2010_08