Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 15859426 | HCID 15859426 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178437930 | HCID 178437930 | 79% |
Reaction Steps
In a 500-ml glass-made reactor equipped with a thermometer and a reflux condenser, 200 ml of n-butanol, 37.5 g of zinc chloride and 50.7 g of sodium azide were charged, followed by stirring for 30 minutes. To the reactor, 50 g of 5-ethyl-2-imino-3-(2'-cyanobiphenyl-4-yl)methyl-1,3,4-thiadiazoline were charged further, followed by heating the internal temperature to 110 to 120° C. at which the reaction was effected for 20 hours. After the completion of the reaction, the reaction mixture was cooled. After the internal temperature decreased to 100° C. or lower, adequate amounts of chloroform and 10% sulfuric acid were added to the reaction mixture, followed by stirring for 30 to 60 minutes. The reaction mixture was cooled and then separated. To the organic layer, a 5% aqueous solution of sodium hydroxide was added. The resulting mixture was stirred for several hours, followed by separation into layers. The aqueous layer was adjusted to pH 7 with 3N hydrochloric acid. The white crystals so precipitated were collected by filtration. The crude crystals so obtained were washed with chloroform under heating and then cooled to room temperature. After cooling to room temperature, the reaction mixture was collected by filtration and dried, whereby about 44.8 g of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05912353 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-0673c82a484d4dd48e9bd02618f70f60 |
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| Source note | uspto-grants-1999_06 |
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