HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 14624273, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 2-Furanacetonitrile, alpha-amino- | HCID 11147706 | — |
| Reactant | HCID 15107290 | HCID 15107290 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 14624273 | HCID 14624273 | 80.8% |
Reaction Steps
2.80 g of alpha-(2-furyl)-alpha-aminoacetonitrile and 6.0 g of triethylamine were dissolved in 50 ml of ethyl acetate, and with stirring, 2.1 g of the 2,4-diethylthiazole-5-carboxylic acid chloride was added dropwise, and the mixture was stirred at room temperature for 1 hour. Water (150 ml) was added, and the precipitated triethylamine hydrochloride was dissolved. The ethyl acetate layer was separated, washed with water and dried over sodium sulfate. The dried ethyl acetate layer was evaporated under reduced pressure to remove the solvent. The residue was recrystallized from n-hexane to give 2.41 g (yield 80.0%) of the desired N-(alpha-cyanofurfuryl)-2,4-dimethylthiazole-5-carboxylic acid amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04980363 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-56e9a72b40954118943b559787322d84 |
| Source note | uspto-grants-1990_12 |