HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromopentane → Biphenyl-4-sulfonic acid-(4-hydroxybutyl)-pentyl-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromopentane | HCID 8057 | — |
| Reactant | N-(4-Hydroxybutyl)[1,1'-biphenyl]-4-sulfonamide | HCID 16094717 | — |
| Product | Biphenyl-4-sulfonic acid-(4-hydroxybutyl)-pentyl-amide | HCID 11552548 | — |
Reaction Steps
Using a method analogous to that described in Example 4, with biphenyl-4-sulfonic acid-(4-hydroxybutyl)-amide and bromopentane, reacted at 60° C. for 3 hours, the title compound was obtained as an amorphous white solid. δC (CDCl3, 62.9 MHz): 14.0, 22.3, 25.3, 28.4, 29.6, 48.1, 48.4, 62.2, 127.3, 127.6, 128.4, 129.0, 138.5, 139.4 and 145.2. δH (CDCl3, 250 MHz): 0.84 (3H, t, J 7.0), 1.24 (4H, m), 1.50 (6H, m), 2.06 (1H, s), 3.14 (4H, m), 3.62 (2H, t, J 5.95), 7.41 (3H, m), 7.56 (2H, d, J 7.94), 7.67 (2H, d, J 8.55) and 7.83 (2H, d, J 8.24).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07964643B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-bb5c73bf89f244919fe3f47596e4d6d2 |
| Source note | uspto-grants-2011_06 |