HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 20263956, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 20263993 | HCID 20263993 | — |
| Reactant | HCID 20381866 | HCID 20381866 | — |
| Product | HCID 20263956 | HCID 20263956 | — |
Reaction Steps
To an ice cold mixture of 0.01 mole of ethylmercapto acetate and 0.02 mole of sodium ethoxide in 100 ml. ethanol under nitrogen is added a solution of 4-bromo-3-hydroxy-2-methyl-5-vinylpyridine hydrobromide in 50 ml. of ethanol. The reaction mixture is stirred overnight at room temperature, concentrated in vacuo and taken up between ethyl acetate and water. The organic layer is separated, washed well with water, dried and concentrated. Chromatography of the residue on silica gel-elution with ether-petroleum ether 10-50% gives 4-ethoxycarbonylmethylthiomethyl-3-hydroxy-2-methyl-5-vinyl pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04217352 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-4644b554dfc943aeae02af4f309b8171 |
| Source note | uspto-grants-1980_08 |