HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482175Generated: October 28, 2026
Lithium → Cholan-24-oic acid, 3-oxo-, methyl ester, (5alpha)-
https://huagongshe.com/reaction/482175
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium | HCID 3028194 | — |
| Reactant | 3-Oxochol-4-en-24-oic acid methyl ester | HCID 11036480 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Cholan-24-oic acid, 3-oxo-, methyl ester, (5alpha)- | HCID 22821830 | 41.8% |
Reaction Steps
Into a solution of 3-oxo-4-cholenic acid methyl ester 3002 (13.0 g, 23.68 mmol) in dry ether (50 ml) was added distilled liquid ammonia (70 ml) at -78° C. Lithium (1.0 g, 144.1 mmol) was added in small portions until a blue coloration persisted for 10 minutes, after which the solution was quenched with solid NH4Cl (50 g). Ammonia was evaporated, and the resulting residue was partitioned between water (100 ml) and ether (150 ml). The aqueous solution was extracted further with ether (3×50 ml). The combined extracts were washed with brine (1×70 ml), dried (MgSO4), filtered and concentrated in vacuo to get the crude product. Flash chromatography of the crude product in silica gel using ethyl acetate:hexane (2:8) gave pure 3-oxo-5α-cholanic acid methyl ester 3003 (3.85 g, 29%). 1H NMR (400 MHz, CDCl3) δ: 0.69 (3H, s, 18-CH3, 0.91 (3H, d, 21-CH3), 1.02 (3H, s, 19-CH3) and 3.66 (3H, s, CO2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05792635 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-8600318e48d4483d82c8ec25fc8b0ec0 |
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| Source note | uspto-grants-1998_08 |
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