HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 21-Bromo-3beta-hydroxypregna-5,16-dien-20-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 16-Dehydropregnenolone | HCID 92871 | — |
| Reactant | 5,5-Dibromobarbituric acid | HCID 94877 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 21-Bromo-3beta-hydroxypregna-5,16-dien-20-one | HCID 10644269 | 104.4% |
Reaction Steps
Dissolve 16-dehydropregnenolone (5.00 g, 15.90 mmol) and 5,5-dibromobarbituric acid (4.55 g, 15.90 mmol) in tetrahydrofuran (60 mL). Add concentrated aqueous hydrogen bromide (100 μL of a 48% solution) to the stirring solution and heat the reaction at reflux for 1 hour. Cool slightly and then concentrate under vacuum to produce a brown oily foam. Dissolve the residue in methylene chloride (350 mL), rinse with 50% saturated sodium bicarbonate (2×200 mL), brine (125 mL), dry over anhydrous magnesium sulfate, filter and concentrate under vacuum to provide 21-bromo-3β-hydroxypregna-5,16-dien-20-one (6.53 g) as an orange-brown solid, slightly contaminated with starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05677293 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-f2f1fb21b46f4ac8904c3542b7de7a3a |
| Source note | uspto-grants-1997_10 |