HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalimide → Phthalimide, N-(2-formylethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Acrolein | HCID 7847 | — |
| Reactant | Tetrabutylammonium Hydroxide | HCID 2723671 | — |
| Product | Phthalimide, N-(2-formylethyl)- | HCID 75525 | — |
Reaction Steps
3-Phthalimidopropanal was prepared by addition of phthalimide to acrolein in the presence of tetrabutylammonium hydroxide according to the procedure described by R. O. Atkinson & F. Poppelsdorf, J Chem. Soc. (1952) 2448. 1H-NMR (CDCl3, 400 MHz): δ 9.82 (t, 1H, J=2); 7.85 (m, 2H); 7.72 (m, 2H); 4.04 (t, 2H, J=7); 2.88 (dt, 2H, J=2, 7). 13C-NMR (CDCl3, 100 MHz): δ 199.36, 167.98, 134.10, 131.95, 123.36, 42.35, 31.67.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492562B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-5e7aab2d130d4159aa86ffb36a53bae1 |
| Source note | uspto-grants-2002_12 |