HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butylamine → N-Butyl-3-methyl-1,2,4-thiadiazol-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | 5-Chloro-3-methyl-1,2,4-thiadiazole | HCID 12919159 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-Butyl-3-methyl-1,2,4-thiadiazol-5-amine | HCID 20393662 | — |
Reaction Steps
5-Chloro-3-methyl-1,2,4-thiadiazole (27 g, 0.20 mol) was dissolved in 200 ml ethanol and, under cooling in an ice bath, added to an ethanolic solution of butylamine (44 g, 0.60 mol), stirred at room temperature overnight and evaporated to small bulk. Upon addition of ether a white precipitate of butylamine hydrochloride formed which was filtered off. The yellow filtrate was washed with water, dried over magnesium sulphate, filtered and evaporated to dryness to yield a yellow oil which was distilled under vacuum to give 5-butylamino-3-methyl-1,2,4-thiadiazole as a pale yellow liquid. Yield 29.9 g, (87.2%), b.p. 101°-102° C./0.14 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163048 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-38ba3b5369844f33ab96af77827abde7 |
| Source note | uspto-grants-1979_07 |