HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 21-Bromo-3alpha-hydroxy-5beta-pregnan-20-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Pregnanolone | HCID 31402 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 21-Bromo-3alpha-hydroxy-5beta-pregnan-20-one | HCID 86754251 | — |
Reaction Steps
To a flask containing a solution of 3α-hydroxy-5β-pregnan-20-one (5.15 g, 16.5 mmol) in methanol (100 mL) was added a solution of bromine (1.1 mL) in methanol (30 mL) dropwise in such a rate to maintain the brown color of the bromine until this color was persistent. Then water (200 mL) was added and the mixture was extracted with CH2Cl2 (3×100 mL). The combined extracts were dried over Na2SO4. Removal of the solvent resulted in the product as a foamy white solid (6.63 g). Other 21-bromo-pregnan-20-ones (3β-ethynyl-3α-hydroxy-21-bromo-5β-pregnan-20-one, 3β-methyl-3α-hydroxy-21-bromo-5α-pregnan-20-one and 3α-hydroxy-3β-trifluoromethyl-12-bromo-5β-19-norpregnan-20-one) were synthesized using the same method.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05939545 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-b46e31347cb04b3faeb53fb156ba3847 |
| Source note | uspto-grants-1999_08 |