HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexylamine → HCID 18539322, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexylamine | HCID 8102 | — |
| Reactant | 1-Bromo-4-tert-butylbenzene | HCID 77595 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18539322 | HCID 18539322 | 99.6% |
Reaction Steps
According to the general procedure B, 4-tert-butylbromobenzene (214 mg, 1.00 mmol) reacted with n-hexylamine (66 μl, 0.50 mmol) using 1 mol % of Pd(OAc)2, 2 mol % of Ph5FcP(t-Bu)2, and sodium tert-butoxide (116 mg, 1.21 mmol) in toluene at 100° C. for 4 h to give the title compound (182 mg, 99%) as an oil: 1H-NMR (400 MHz, CDCl3): δ 7.17 (d, 4H, J=8.4Hz), 6.82 (d, 4H, J=8.8 Hz), 3.55 (t, 2H, J=7.2 and 8.0 Hz), 1.57 (m, 2H), 1.22 (s, 18H), 0.79 (t, 3H, J=6.4 and 6.8 Hz). 13C{1H}-NMR (100 MHz, CDCl3): δ 145.68, 143.41, 125.93, 120.20, 52.38, 34.06, 31.67, 31.49, 27.55, 26.78, 22.70, 14.05. GC/MS(EI): m/z 365 (M+). Anal. Calcd for C26H39N: C, 85.42; H, 10.75; N, 3.83. Found: C,85.22; H, 10.82; N, 3.86.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562989B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-4c48852a10bb4498996e0ea7f5eb2ed9 |
| Source note | uspto-grants-2003_05 |