HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethanol → HCID 54115112, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Sulfanylandrost-5-en-17-one | HCID 237644 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54115112 | HCID 54115112 | — |
Reaction Steps
To a solution of 2.0 g of 3β-mercapto-androst-5-en-17-one (Swann D. A. and Turnbull J. H., Tetrahedron, 1966, 22, 231) and 0.33 ml of 2-chloroethanol in 5.0 ml of tetrahydrofuran under nitrogen atmosphere at room temperature, 0.030 g of sodium hydride (60% dispersion in mineral oil) were added. The reaction mixture was stirred for 3 hrs, diluted with water and extracted with ethyl acetate; the organic layer was dried over sodium sulfate and evaporated to dryness under reduced pressure. The crude product was purified by flash-chromatography (SiO2) using methylene chloride/methanol/30% ammonia solution 95/5/1 as eluant to give 1.2 g of 3β-(2-hydroxyethylthio)-androst-5-en-17-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521167 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-586fd431d3ed4bcb9914c3bc1ccf5fd7 |
| Source note | uspto-grants-1996_05 |