HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 54504397, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 54477411 | HCID 54477411 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54504397 | HCID 54504397 | — |
Reaction Steps
In 30 ml. of ethanol are dissolved 1 g. of 3-ethoxy-6-formylandrosta-3,5-diene according to reaction (2), and while the solution is stirred at room temperature, 0.1 g. of sodium borohydride is added. After 20 minutes, the reaction mixture is poured into water and extracted with ether. Then, the extract is washed with water and dried with anhydrous sodium sulfate. Finally the solvent is concentrated, whereupon 1 g. of 3-ethoxy-6-hydroxymethylandrosta-3,5-diene is obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03953483 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-0163dbaa89d84bef9e0ca9913aea4d21 |
| Source note | uspto-grants-1976_04 |