Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpyrrole | HCID 7304 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11040770 | HCID 11040770 | 93.2% |
Reaction Steps
Under nitrogen atmosphere, to a mixture of 25.08 g of KSCN (0.125 mole) in 60 ml dry methanol chilled to -78° C. was added dropwise 20 g of Br2 (in 40 ml methanol). The resulting yellow solution was stirred for 5-10 minutes and 10.1 g (0.125 mole) of the 1-methylpyrrole added in one portion. The mixture was allowed to warm to ambient temperature and stirred for one hour. The mixture was poured into 600 ml of ice-water, extracted 2 times with 300 ml CH2Cl2. The CH2Cl2 extract was dried and concentrated to 16.1 g (90% yield) of 1-methyl-5-cyanothiopyrrole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04434175 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-b6bf786f4ef54ebf90c1acaa68afbdb0 |
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| Source note | uspto-grants-1984_02 |
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