HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-3-pyridinecarboxaldehyde → 2-((4-Chlorophenyl)sulfonyl)nicotinaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-3-pyridinecarboxaldehyde | HCID 737607 | — |
| Reactant | Sodium 4-chlorobenzenesulfinate | HCID 23664783 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-((4-Chlorophenyl)sulfonyl)nicotinaldehyde | HCID 59380592 | 46.9% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
2-Chloro-3-pyridinecarboxaldehyde (5.0 g, 35.0 mmol) and 4-chlorobenzenesulfinic acid sodium salt (7.75 g, 38.8 mmol) were dissolved in DMSO (120 ml) and the mixture was heated at 100° C. for 72 h under nitrogen. Upon cooling to ambient the mixture was diluted with water (500 ml) and extracted with EtOAc (3×). The combined organics were washed with water, brine, dried (MgSO4) and evaporated to dryness to afford 8.1 g of crude material. The crude compound was pre-absorbed onto silica and purified by dry pad suction column chromatography, eluting with heptane using an EtOAc gradient, to afford 4.62 g (61%) of the desired product as a white powdery solid (MP=100.5-101° C.; IR=1698 cm−1; HPLC=8.00 min>99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919512B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-2acd1e7f2fba495fb7470d32ab3b91a4 |
| Source note | uspto-grants-2011_04 |