HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618870Generated: November 1, 2026
Potassium Carbonate → HCID 70048161, compound
https://huagongshe.com/reaction/618870
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23238953 | HCID 23238953 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 70048161 | HCID 70048161 | — |
Reaction Steps
A solution of 10.0 g of 3β-acetoxy-5β-pregn-14-en-20-one (Bach, G. et al. Can. J. Chem. 1968, 46, 733) and K2CO3 (25.0 g) in MeOH/water (160 mL/80 mL) was stirred at room temperature for 2 hrs; the organic solvent was evaporated to dryness under reduced pressure and the aqueous suspension obtained was extracted with CH2Cl2 ; the organic layer was dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure; the crude 3β-acetoxy-5β,17α-pregn-14-en-20-one obtained was used for the next step without further purification. A solution of the crude intermediate and p-toluensulphonyl hydrazide (11.1 g) in AcOH (300 mL) was stirred at room temp. for 12 hrs. To this solution NaBH4 (7.8 g) was added portionwise; after 2 hrs the reaction mixture was poured in water/ice and the aqueous suspension obtained was extracted with AcOEt and neutralised with 0.1 N NaOH: the organic layer was dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by flash-chromatography (SiO2) using n-hexane/ethyl acetate 1/1 as eluant to give 7.0 g of 3β-acetoxy-5β,17α-pregn-14-ene as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05955632 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-8aaf24e7b2f54ea98d59a283c7f265f9 |
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| Source note | uspto-grants-1999_09 |
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