HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropyl Ether → HCID 10220113, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 3,5-Dinitroaniline | HCID 12068 | — |
| Reactant | 3-Bromo-2-methyl-1-propene | HCID 357785 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10220113 | HCID 10220113 | — |
Reaction Steps
To a solution of t-butylnitrite (0.13 ml, 1.1 mmol) and 3-bromo-2-methylpropene (0.82 ml, 8.25 mmol) in 1 ml CH3CN, 3,5-dinitroaniline (0.10 g, 0.55 mmol) was added at room temperature. The solution was stirred for 17 h at room temperature and then isopropylether was added. The suspension was filtered through a pad of Al2O3. The volatile material in the solution was removed at reduced pressure to give the title compound. 1H-NMR (CDCl3, 300 MHz) δ ppm: 8.92 (t, J=2.1 Hz, 1H), 8.40 (d, J=2.1 Hz, 2H), 5.00 (s, 1H), 4.82 (s, 1H), 3.55 (s, 2H), 1.72 (s, 3H). 13C-NMR (CDCl3, 75.43 MHz) δ ppm: 148.4, 144.2, 142.0, 129.0, 116.9, 114.8, 43.9, 22.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06284894B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-8290b514611a4a279456410e51c327d9 |
| Source note | uspto-grants-2001_09 |