HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 23676784, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 15187623 | HCID 15187623 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23676784 | HCID 23676784 | 100.5% |
Reaction Steps
In a 50 ml flask, sodium hydride (60% in oil) (200 mg, 5 mmol) and tetrahydrofuran (10 ml) were charged, and then 4,6-dimethylpyridine-2-sulfonic acid (935 mg) was gradually added at room temperature. Then, the mixture was stirred at room temperature for about 30 minutes. After the addition of a small amount of ethanol to the reaction mixture, the precipitated crystal was recovered by filtration. The crystal was washed with ethyl acetate and diethyl ether successively and dried to obtain sodium 4,6-dimethyl-2-pyridinesulfonate (1.05 g) at a quantitative yield. Melting point, 257°-258° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374732 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-46b2f6d4d27b4dd2b368623753aaa1c8 |
| Source note | uspto-grants-1994_12 |