HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 67019559, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 3-(4-Chlorosulfonyl-phenyl)-acrylic acid | HCID 3830969 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67019559 | HCID 67019559 | 54.3% |
Reaction Steps
To a mixture of aniline (0.35 g, 3.75 mmol) and pyridine (1 ml) a solution of 3-(4-chlorosulfonyl-phenyl)acrylic acid (42) (0.45 g, 1.82 mmol) in dichloromethane (3 ml) was added and the resultant solution was stirred at 40° C. for 1 hour. The reaction mixture was evaporated and the residue was partitioned between ethyl acetate and 6N HCl. The organic layer was washed successively with water, saturated NaCl and dried (Na2SO4). The solvent was evaporated under reduced pressure to give the title compound (0.30 g, 54%). 1H NMR (DMSO-d6, HMDSO), δ: 6.60 (1H, d, J=16.0 Hz); 6.93–7.43 (5H, m); 7.60 (1H, d, J=16.0 Hz); 7.79 (2H, d, J=8.0 Hz); 7.87 (2H, d, J=8.0 Hz); 10.35 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183298B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-dc320e661eb14102923742d367a4071a |
| Source note | uspto-grants-2007_02 |