HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20475365, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 20475368 | HCID 20475368 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 20475365 | HCID 20475365 | — |
Reaction Steps
1.4 g (5.8 mmols) of 3-methyl-6-acetoxymethyl-2,2'-bipyridine are boiled under reflux for 30 minutes in a mixture of 20 ml of 10% sodium hydroxide solution and 15 ml of ethanol. After cooling, the mixture is acidified with hydrochloric acid and washed with twice 20 ml of ethyl acetate. The aqueous phase is rendered alkaline with potassium carbonate, and the reaction product is extracted with 40 ml of ethyl acetate. After drying over sodium sulfate and concentration in vacuo, the 3-methyl-6-hydroxymethyl-2,2'-bipyridine is crystallised from diethyl ether. Yield: 0.99 g (85% of theory); melting point 51°-53° C. UV absorption (in chloroform): λmax =281 nm (ε=9400).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04424359 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-154de8da489945edbee2068994b2c872 |
| Source note | uspto-grants-1984_01 |