HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4-methylthiazole → HCID 44313067, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4-methylthiazole | HCID 74143 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 11116082 | HCID 11116082 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 44313067 | HCID 44313067 | — |
Reaction Steps
In 170 ml of benzene, 4.45 l g (0.035 mole) of 3,3-dimethylglutaraldehyde was combined with 3.96 (0.035 mole) of 2-amino-4-methylthiazole under nitrogen. The reaction mixture was brought to reflux and water azeotroped off via a Dean-Stark trap. After 21 hours 0.20 g (0.001 mole) of p-toluenesulfonic acid monohydrate was added to the reaction mixture and heating continued an additional 5 hours after which the solvent was evaporated in vacuo. The crude product was purified by silica gel flash chromatography eluting with a 1% ethyl acetate/hexane solution. The eluate was evaporated in vacuo to yield 2.67 g of the title compound as a clear liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742068 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-a24052bfa0d9458dacd422d09761998e |
| Source note | uspto-grants-1988_05 |