HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrole-2-carboxaldehyde → HCID 136495273, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrole-2-carboxaldehyde | HCID 13854 | — |
| Reactant | 2-[Di(propan-2-yl)phosphanyl]ethan-1-amine | HCID 57552996 | — |
| Product | HCID 136495273 | HCID 136495273 | 97.2% |
Reaction Steps
Replicate the preparation of the ligand used in Ex. 7 except use 0.2 g (2.103 mmol) of pyrrole-2-carbaldehyde and use adding 0.356 g (2.208 mmol) of 2-(di-isopropylphosphino)ethanamine instead of N1,N1-dimethylethane-1,2-diamine to give 0.487 g (97%) of N-((1H-pyrrol-2-yl)methylene)-2-(di(propan-2-yl)phosphino)ethanamine as a colorless, semi solid, which is analytically pure by GC-MS and 1H-NMR: 1H NMR (400 MHz, Benzene): δ 10.05 (s, 1H), 7.83 (s, 1H), 6.51 (s, 1H), 6.44 (m, J=2.2 Hz, 1H), 6.28-6.14 (m, 1H), 3.67 (dd, J=15.2, 6.9 Hz, 2H), 1.75-1.64 (m, 2H), 1.58 (dq, J=6.9, 5.3 Hz, 2H), 1.00 (ddd, J=14.8, 12.3, 7.1 Hz, 12H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422375B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-e5e25d90a67c48d9af0c0b0bb3cd9bb1 |
| Source note | uspto-grants-2016_08 |