HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl isocyanate → N-(1-cyanoethyl)-N'-(1,1-dimethylethyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl isocyanate | HCID 62412 | — |
| Reactant | Propanenitrile, 2-amino- | HCID 411840 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(1-cyanoethyl)-N'-(1,1-dimethylethyl)urea | HCID 21316847 | — |
Reaction Steps
To a stirring solution of 21.1 g (0.3 mole) 2-aminopropionitrile in 300 ml. dry tetrahydrofuran under a nitrogen atmosphere, there is added 30.7 g (0.3 mole) t-butyl isocyanate (97%). The resulting mixture is heated at reflux for five hours. At the end of this period, the tetrahydrofuran is removed at reduced pressure. The solid is recrystallized from methanol:water, 60:40, to give N-(1-cyanoethyl)-N'-(1,1-dimethylethyl)urea, m.p. 161°-3°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04156738 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-f6408094509d48d58ea659d4a8ff15bc |
| Source note | uspto-grants-1979_05 |