HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507682Generated: October 27, 2026
Dimethyl Sulfide → HCID 57428875, compound
https://huagongshe.com/reaction/507682
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | N,N-Diethyl-para-anisamide | HCID 231459 | — |
| Reactant | HCID 178511841 | HCID 178511841 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57428875 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07786132B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-9eaf5759cfb642039848c8751e9e1b0f |
|---|
| Source note | uspto-grants-2010_08 |
|---|