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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457477Generated: October 31, 2026

Lithium → Cholan-24-oic acid, 3-oxo-, methyl ester, (5alpha)-

https://huagongshe.com/reaction/1457477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithiumHCID 3028194—
Reactant3-Oxochol-4-en-24-oic acid methyl esterHCID 11036480—
ReactantEthyl acetate hexaneHCID 21226206—
SolventDiethyl EtherHCID 3283—
ProductCholan-24-oic acid, 3-oxo-, methyl ester, (5alpha)-HCID 2282183041.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05847172
Source datasetuspto-grants-1998_12
ORD IDord-f1760c76c6264b16898f7d6a8ec04acc
Source noteuspto-grants-1998_12