HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2-Methyl-3-hydroxy-4-mercaptomethyl-5-vinylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ether tetrahydrofuran | HCID 21868444 | — |
| Reactant | HCID 178437128 | HCID 178437128 | — |
| Product | 2-Methyl-3-hydroxy-4-mercaptomethyl-5-vinylpyridine | HCID 13066946 | — |
Reaction Steps
The isothioureido compound from Example 25, Step A, (0.1 mole) in 200 ml. of tetrahydrofuran:ether (3:1 v/v) is added to excess lithium aluminum hydride under ether and nitrogen at 0° C. over 30 minutes. After stirring one hour at room temperature, it is poured into a mixture of tetrahydrofuran and saturated ammonium chloride solution. The water layer is separated and extracted with 2×400 ml. of tetrahydrofuran. The combined tetrahydrofuran solutions are dried and evaporated to dryness to give 2-methyl-3-hydroxy-4-mercaptomethyl-5-vinylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04355034 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-ab808fc495a84753b32b1df2c9a5c120 |
| Source note | uspto-grants-1982_10 |