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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 14816496 | HCID 14816496 | — |
| Reactant | HCID 178437674 | HCID 178437674 | — |
| Product | 5-(3,5-Dimethylphenylthio)-4-ethyl-2-methyl-1-trimethylsilyloxyethoxymethyl-imidazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05326780 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-541c299343c54ee59e2ee5e7a1a83ac5 |
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| Source note | uspto-grants-1994_07 |
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