Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Furfurylamine | HCID 3438 | — |
| Reactant | HCID 178503391 | HCID 178503391 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178478539 | HCID 178478539 | — |
Reaction Steps
A mixture consisting fo 6.0 gm (0.0202 mol) of 2-methylmercapto-4-(2',6'-dichloro-phenyl)-2-imidazoline hydrochloride and 2.8 gm (0.029 mol) of furfurylamine was heated for 30 minutes at 140° C. The resulting dark-brown mass was dissolved in ethanol and then crystallized by addition of acetone and ether; for further purification, the crystallizate was again dissolved in ethanol and acetone, reprecipitated by addition of ether, and recrystallized from water, yielding 2.5 gm (35.7% of theory) of the yellow crystalline compound of the formula ##STR12## which had a melting point of 191° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04080503 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-00f45f03f19541f283adbbe1f24ab6cf |
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| Source note | uspto-grants-1978_03 |
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