HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 3-tert-Butyldimethylsilyloxy Pregnenolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Pregnenolone | HCID 8955 | — |
| Reactant | tert-Butyldimethylsilyl trifluoromethanesulphonate | HCID 123564 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-tert-Butyldimethylsilyloxy Pregnenolone | HCID 10884505 | — |
Reaction Steps
Imidazole (ImH) can be added to a solution of pregnenolone (compound 3, see Scheme 1) in anhydrous dimethylformamide (DMF). Tert-butyldimethylsilyltrifluoromethanesulfonate can then be added to the solution. The reaction product can be purified to obtain compound 4, 1-((3S,8S,9S,10R,13S,14S,17S)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3-[(1,1-dimethylethyl)dimethylsilyloxy]-10,13-dimethyl-1H-cyclopenta[α]phenanthren-17-yl) ethanone, as shown in Scheme 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022052B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-3f85b035e8f748f09b57c7667340d385 |
| Source note | uspto-grants-2011_09 |