Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chloromethyl methyl sulfide | HCID 16916 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22821721 | HCID 22821721 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22821723 | HCID 22821723 | — |
Reaction Steps
To a suspension of cis-7-chloro-3-hydroxy-2,3-dihydro-2-(1'-imidazolylmethyl)benzo(b)thiophene (2.67 gms., 10 mmols) in dry dimethylformamide (30 ml.) at 0°-5° C., add sodium hydride (50% oil dispersion) (0.53 gms., 11 mmols) and stir for one hour at room temperature. Add chloromethyl methyl sulfide (1.06 gms., 11 mmols) and stir again for one hour at room temperature. Pour the reaction mixture into ether (500 ml.) and extract with three portions (500 ml. each) of water. Dry the ether solution over anhydrous magnesium sulfate and evaporate in vacuo. Chromatograph the resultant residue by high pressure liquid chromatography using two silica gel cartridges and eluting with ethyl acetate. Combine the like eluates as determined by thin layer chromatography and evaporate the combined residues to give cis-7-chloro-3-(methylthiomethoxy)-2,3-dihydro-2-(1'-imidazolylmethyl)benzo(b)-thiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04352808 |
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| Source dataset | uspto-grants-1982_10 |
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| ORD ID | ord-0bd17da7b7ac479e82636a68c759e75e |
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| Source note | uspto-grants-1982_10 |
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