HuagongsheHuagongshe Chemistry Print Report · For research reference only
Naphthalene → 5-Chloro-pyridine-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | 3-chloro-5-formyl-2H-pyridine-1-carboxylic acid phenyl ester | HCID 57565931 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Chloro-pyridine-3-carbaldehyde | HCID 14444196 | — |
Reaction Steps
The mixture of 3-chloro-5-formyl-2H-pyridine-1-carboxylic acid phenyl ester (2.3 g, 8.8 mmol), sublimed sulfur (0.29 g, 9 mmol) and naphthalene (6 g) was refluxed under an argon atmosphere for 2 h. After the reaction was complete, the mixture was cooled to r.t., dissolved in ethyl ether (30 mL), and extracted with aqueous 10% HCl. The combined acid extracts were washed with ethyl ether (20 mL) and cooled to 0° C. Dichloromethane (30 mL) was added and “pH” of the mixture was adjusted to be basic with 25% aqueous NaOH, and the mixture was extracted with dichloromethane (20 mL). The combined organic phase was washed with brine, dried over K2CO3, filtered, and concentrated to give a brown solid. (0.8 g, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07495007B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-58e86f768a244136a67dc6224cf5b5d3 |
| Source note | uspto-grants-2009_02 |