HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232806Generated: October 30, 2026
Water → 3alpha-N-methyl-dihydronicotinoyloxy-5alpha-pregnan-20-one
https://huagongshe.com/reaction/232806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3alpha-N-methyl-nicotinoyloxy,5alpha-pregnan-20-one iodide | HCID 131718039 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3alpha-N-methyl-dihydronicotinoyloxy-5alpha-pregnan-20-one | HCID 67710668 | — |
Reaction Steps
To an ice cold solution of the 3α-N-methyl-nicotinoyloxy-5α-pregnan-20-one iodide salt (1.01 g, 562 g/m, 1.8 mmol) in 150 mL of aqueous methanol (100 mL methanol and 50 mL water, deaerated) was added sodium bicarbonate (620 mg, 84 g/m, 7.4 mmol) and sodium dithionite (1.3 g, 174 g/m, 7.4 mmol). This mixture was stirred at 0° C. for 1 h. The reaction mixture was poured into 500 mL of water and extracted several times with chloroform. The combined organic layers were washed with potassium carbonate and concentrated. The crude product was filtered through a bed of silica gel using hexane/ethyl acetate (5:1) elution. The product was recovered in the initial fractions to give 180 mg (439 g/m, 0.4 mmol, 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05591733 |
|---|
| Source dataset | uspto-grants-1997_01 |
|---|
| ORD ID | ord-c9c6106a5d75431cacdb79033dae1978 |
|---|
| Source note | uspto-grants-1997_01 |
|---|