Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 54246468 | HCID 54246468 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22788009 | HCID 22788009 | — |
Reaction Steps
To a solution of 116 parts of 3-methoxyspiro[estra-1,3,5(10)-triene-17,2'(5'H)-furan] in 1100 parts of tetrahydrofuran at 5°-10° under nitrogen is added, with stirring, a solution of approximately 5 parts of borane in 325 parts of tetrahydrofuran. Stirring at 5°-10° is continued for 21/4 hours, whereupon a solution of 26 parts of sodium hydroxide in 213 parts of water followed -- cautiously -- by 131 parts of 30% hydrogen peroxide is mixed in. The resultant mixture is acidified with 20% hydrochloric acid and then poured into 7000 parts of ice water. The precipitate which forms is isolated by filtration, washed with water, dried in air, and taken up in benzene. The benzene solution is chromatographed on silica gel, using benzene and mixtures thereof with increasing amounts of ethyl acetate as developing solvents. From an eluate comprising 10% ethyl acetate in benzene, on evaporation of solvent and recrystallization of the residue from ethyl acetate, 4' ,5'-dihydro-3-methoxyspiro[estra-1,3,5(10)-triene-17,2'(3'H)-furan]-4'-ol melting at 95°-97° is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03939155 |
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| Source dataset | uspto-grants-1976_02 |
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| ORD ID | ord-4fb1db7e1bc840d589f093f7404bea0b |
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| Source note | uspto-grants-1976_02 |
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