Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 57237521 | HCID 57237521 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86737779 | HCID 86737779 | 68.3% |
Reaction Steps
To a solution of 14 (22.0 g, 70 mmole) in 95% ethanol (200 ml) was added concentrated HCl (12 ml) and 10% palladium on activated carbon (2.0 g). The mixture was hydrogenated at an initial pressure of 50 psi until the uptake of hydrogen ceased. The mixture was filtered from the catalyst and the filtrate evaporated to a small volume. The residue was dissolved in water, the solution made basic with concentrated NH4OH and extracted with three portions of chloroform. The chloroform extracts were washed with dilute NH4OH, dried and evaporated to a thick syrup which crystallized on the addition of ethyl acetate. The crystals were collected and dried to give 14.4 g (65%) of 16a as white needles, mp 163°-165°. Recrystallization from acetone gave analytically pure 16a as the hemi-acetone solvate, 166°-167° NMR: δ 6.55, s, 2H (aromatic); 6.40, broad, 1H (hydroxyl H); 4.22, d, 1H (H-5α, J=13 Hz); 3.77 (CH3O--); 2.38 (CH3N); 0.87, d, 3H (7α-CH3, J=6.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04272541 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-0b3c64b4c3424e658e22170846b8ca53 |
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| Source note | uspto-grants-1981_06 |
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