HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitroethane → HCID 68527591, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitroethane | HCID 6587 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Cyclohepten-1-one | HCID 70723 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68527591 | HCID 68527591 | — |
Reaction Steps
To a solution of 80% technical grade 2-cycloheptenone (3.48 mL, 25 mmol) and triethylamine (1 mL) in toluene were added phenylisocyanate (5.95 g, 50 mmol) and nitroethane (2.24 g, 30 mmol) in four portions over 1 hour. The reaction mixture was stirred at ambient temperature for 4 hours, the precipitate was filtered off and the filtrate was concentrated. The obtained residue was chromatographed, eluting with 20% ethyl acetate/hexane to yield the title compound: 1H NMR (300 MHz, CDCl3) δ 4.81 (m, 1 H), 4.06 (d, J=11.87 Hz, 1 H), 2.47 (m, 2 H), 2.02 (m, 3 H), 1.93 (m, 2 H), 1.81 (m, 2 H), 1.67 (m, 2 H); MS (DCI/NH3) m/z 168 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546410B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-2462051d1df64fe3b7c730616b25980b |
| Source note | uspto-grants-2013_10 |