Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | HCID 21490114 | HCID 21490114 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21490111 | HCID 21490111 | — |
Reaction Steps
1-(α-Chloroacetyl)-2,5-dimethylpyrrolidine (10 grams; 0.057 mol), potassium thiocyanate (10.1 grams), sodium iodide (a few crystals) and ethanol (100 ml) were charged into a glass reaction flask equipped with mechanical stirrer and reflux condenser. The reaction mixture was heated at reflux, with stirring, for a period of about 2 hours. After this time the reaction mixture was cooled and filtered. The filtrate was stripped of ethanol under reduced pressure resulting in a solid product. The solid was extracted with two 125 ml portions of hot benzene. The benzene extracts were combined and were evaporated to yield 1-(α-thiocyanoacetyl)-2,5-dimethylpyrrolidine as a light brown oil having a refractive index at 25° C. of 1.5185 and having the following elemental analysis as calculated for C9H14N2OS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03998808 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-003864997c464f9593a6b3add12bd8a3 |
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| Source note | uspto-grants-1976_12 |
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