HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-(2-phenylbenzoyl)-N-isobutylhydrazinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | 2-Methylpropyl isocyanate | HCID 61281 | — |
| Reactant | 2-Phenylbenzhydrazide | HCID 2760365 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-phenylbenzoyl)-N-isobutylhydrazinecarboxamide | HCID 48613827 | — |
Reaction Steps
1.00 g (4.71 mmol) of 2-phenylbenzoic acid hydrazide are placed in 10 ml tetrahydrofuran at room temperature. 0.51 g (5.15 mmol) of isobutyl isocyanate, dissolved in 2 ml tetrahydrofuran, are rapidly added dropwise with stirring. The mixture is firstly stirred further at room temperature and then allowed to stand overnight. Addition of an equal volume of diethyl ether and 10 ml of cyclohexane results in separation of a small quantity of a solid, which is filtered off and discarded. Concentration of the filtrate yields 1.53 g (ca. 100% of theory) of a slightly THF-moist product, which is used further as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084481B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-005a66039c134a6c96c57ede4e85a2c5 |
| Source note | uspto-grants-2011_12 |