Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | 2,5-Dimethyl-1,3,4-thiadiazole | HCID 96922 | — |
| Product | HCID 136139912 | HCID 136139912 | — |
Reaction Steps
570 g (5 moles) of 2,5-dimethyl-1,3,4-thiadiazole and 275 g (2.5 moles) of salicylaldehyde are mixed and the mixture is slowly heated to 150° C. whilst passing nitrogen through it. The mixture is kept at 150° C. for 30 hours and is then cooled, the excess 2,5-dimethyl-1,3,4-thiadiazole is distilled off and the residue is recrystallized from methylglycol. 304 g (56% of theory) of yellow crystals of melting point 253°-254° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04305950 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-16fe359c50f34367a65686e5c592db26 |
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| Source note | uspto-grants-1981_12 |
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