HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylbutanal → N-tert-butyl-C-(2-phenylpropyl)nitrone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylbutanal | HCID 85979 | — |
| Reactant | N-tert-butylhydroxylamine | HCID 98586 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-tert-butyl-C-(2-phenylpropyl)nitrone | HCID 86593654 | 92.8% |
Reaction Steps
To a mixture of 3-phenylbutyraldehyde (10.0 g, 67.5 mmol, 1.0 equiv) and benzene (150 ml) and silica gel (5 g) was added N-tert-butylhydroxylamine (7.22 g, 81.0 mmol, 1.2 equiv) and the mixture stirred at rt for 18 h. The mixture was filtered and the filtrate was concentrated under vacuum to give N-tert-butyl-C-(2-phenylpropyl)nitrone (13.74 g, 92.80%) as a light yellow oil. 1H NMR (CDCl3) δ 7.33–7.19 (m, 5H), 6.65 (t, 1H), 3.18–3.04 (m, 1H), 2.90–2.65 (m, 2H), 1.40 (s, 9H), 1.34–1.32 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115666B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-10ffcbf8f3974b93b3185070f09ec56f |
| Source note | uspto-grants-2006_10 |