HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586810Generated: November 3, 2026
Dimethyl Disulfide → HCID 19759362, compound
https://huagongshe.com/reaction/1586810
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | HCID 19759533 | HCID 19759533 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 19759362 | HCID 19759362 | — |
Reaction Steps
To a mixture of N,N,N'-N'-tetramethylethylenediamine (1.55 ml) and 5-bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)pyrrole-2-carbonitrile (3.80 g) was added dropwise n-butyllithium solution (1.6M solution in n-hexane, 5.2 ml) during a period of 20 minutes at -60° C. under nitrogen atmosphere. The mixture was stirred for one hour at the same temperature and then dimethyldisulfide (1 ml) was added therein in one portion. The reaction mixture was allowed to warm to ambient temperature, stirred overnight at the same temperature and then poured into ice water. The separated oil was extracted with ethyl acetate. The organic layer was washed with water, dried, and concentrated in vacuo to give the residue, which was purified by column chromatography on silica gel to yield 1-(4-tert-butyldiphenylsilyloxymethylphenyl)-5-methylthiopyrrole-2-carbonitrile (1.94 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05215994 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-9f0ab66322c946c7803715c49d637132 |
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| Source note | uspto-grants-1993_06 |
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