HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963172Generated: October 30, 2026
HCID 22875683, compound → HCID 22875682, compound
https://huagongshe.com/reaction/963172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22875683 | HCID 22875683 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Cyclohexanone | HCID 7967 | — |
| Product | HCID 22875682 | HCID 22875682 | — |
Reaction Steps
A solution of 20-tert-butyldimethylsilyloxy-7-methyl-pregn-5-ene-3,7-diol (298 gm, 0.59 mol, product of Step 4) in toluene (3 L) and cyclohexanone (1.03 L) was azeotroped to remove 750 mL of solvent. A solution of aluminum isopropoxide (121 gm) in toluene (620 mL) was added and the solution azeotroped to remove another 650 mL of solvent. A reflux condenser was added and the solution refluxed overnight. The solution was cooled to 40° C. and Supercell™ (125 gm) and water (125 mL) were added. After stirring for 10 min, the mixture was filtered and the solids washed with toluene (550 mL). The solvent was removed by rotoevaporation to yield a orange liquid which was purified by column chromatography on silica gel eluted with hexane, followed by 5-10% ethyl acetate in hexanes. The title compound was isolated as a mixture of 20α- and 20β-isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763361 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-a57e03f3a6714acdb181cd6db1cf9197 |
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| Source note | uspto-grants-1998_06 |
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