Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728332Generated: October 31, 2026

Dimethylformamide → 5-(3,5-Dimethylphenylthio)-4-ethyl-2-methyl-1-trimethylsilyloxyethoxymethyl-imidazole

https://huagongshe.com/reaction/1728332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14816496HCID 14816496—
ReactantHCID 178437674HCID 178437674—
Product5-(3,5-Dimethylphenylthio)-4-ethyl-2-methyl-1-trimethylsilyloxyethoxymethyl-imidazoleHCID 19002951—

Reaction Steps

To a solution of 500 mg of 5-(3,5-dimethylphenylthio)-ethyl-2-methylimidazole (2 mmol) in 5 ml of dry dimethylformamide is added 120 mg of 60% oil suspension of sodium hydride (3 mmol) under ice cooling and allowed to stand for 5 minutes. After the addition of 820 mg of iodomethyl trimethylsilyloxyethyl ether (3 mmol) [Tetrahydron Letters, No. 35, pp. 3263-3264, 1979],the mixture is allowed to stand for 15 minutes, when it is poured onto ice water and extracted with ethyl ether. The extract is washed with water, dried over sodium sulfate, filtered and concentrated in vacuo. The residue is chromatographed on a column of silica gel, eluting with ethyl acetate/n-hexane (2:1) to give 170 mg of 5-(3,5-dimethylphenylthio )-4-ethyl-2-methyl-1-trimethylsilyloxyethoxymethyl-imidazole 4 as an oil. Yield, 21%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05326780
Source datasetuspto-grants-1994_07
ORD IDord-541c299343c54ee59e2ee5e7a1a83ac5
Source noteuspto-grants-1994_07