HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobenzenesulfonamide → 4-[2-(4-Chlorophenyl)phenyl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobenzenesulfonamide | HCID 69696 | — |
| Reactant | 4'-Chlorobiphenyl-2-boronic acid | HCID 23450998 | — |
| Product | 4-[2-(4-Chlorophenyl)phenyl]benzenesulfonamide | HCID 10545354 | 67% |
Reaction Steps
Following the general procedure outlined in Synthetic Scheme IX, 1.6 g (6.9 mmol) of 2-(4-chlorophenyl)phenylboronic acid (Step 2) was reacted with 1.8 g (7.6 mmol) of 4-bromobenzenesulfonamide. Purification by silica gel chromatography (Waters LC-2000) with ethyl acetate/hexane (3:7) and subsequent recrystallization from ethyl acetate/hexane gave 1.59 g (67%) of 4-[2-(4-chlorophenyl)phenyl]benzenesulfonamide as a colorless solid: mp 206.2°-207.0° C.; NMR (CDCl3) δ 4.77 (s, 2H), 7.04 (d, J=9 Hz, 2H), 7.16-7.31 (m, 4H), 7.36-7.51 (m, 4H), 7.80(d, J=9 Hz, 2H). MS (EI): m/e (rel intensity) 343 (100), 308 (13), 262 (21), 228 (82); HRMS Calc'd for C18H14ClNO2S: 343.0434. Found: 343.0434.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05739166 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-cb9377ea27134f42a17e4a2243427bf6 |
| Source note | uspto-grants-1998_04 |