HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 4202153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzenesulfonyl chloride, 4-chloro-3-nitro- | HCID 7323 | — |
| Reactant | 3-Chloroaniline | HCID 7932 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 4202153 | HCID 4202153 | — |
Reaction Steps
A mixture of 4-chloro-3-nitrobenzenesulfonylchloride (1 g, 3.9 mmol), 3-chloroaniline (0.5 mL, 4.7 mmol) and pyridine (1.6 mL) in CH2Cl2 (2 mL) was stirred at room temperature. The reaction was quenched with NaHCO3 (sat aq solution, 30 mL×3). The organic phase was separated, dried (MgSO4), and filtered. The volatiles were evaporated and the residue was purified by column chromatography (SiO2, pentane:EtOAc, 4:1) to give 4-chloro-N-(3-chlorophenyl)-3-nitrobenzenesulfonamide; MS (posESI) m/z=349.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566715B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-f8e3783d49ea418da24a6b54c6ba3c71 |
| Source note | uspto-grants-2009_07 |