HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67578953, compound → HCID 67578508, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67578953 | HCID 67578953 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67578508 | HCID 67578508 | 64.8% |
Reaction Steps
A solution of N-isopropyl-3-(2-allylphenoxy)propylamine hydrobromide (313 mg) in ethanol was hydrogenated at ambient temperature and pressure for 3 hours using a catalyst of palladium on carbon (10% w/w, 30 mg). The catalyst was removed by filtration and the filtrate evaporated to give a solid which was crystallised from a mixture of propan-2-ol and diethyl ether to give N-isopropyl-3-(2-propylphenoxy)propylamine hydrogen bromide as a colourless solid (204 mg), m.p. 89°-90°; microanalysis, found: C, 56.6; H, 8.2; N, 4.43%; C15H25NO.HBr requires: C,57.0; H, 8.3; N, 4.70%; NMR([CD3 ]2SO): 0.92(3H,t), 1.25(6H,d), 1.55(2H,m), 2.10(2H,m), 2.51(2H,m), 3.10(2H,t), 3.31(1H,m), 4.05(2H,t), 6.90(2H,m), 7.13(1H,m) and 8.46(2H,m); m/z 236(M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866611 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-c8bd05d0b6864042a25d22e1d2a6812c |
| Source note | uspto-grants-1999_02 |