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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062921Generated: October 31, 2026

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

https://huagongshe.com/reaction/1062921

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, 29w). 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 numberUS06962909B2
Source datasetuspto-grants-2005_11
ORD IDord-83de01f46a1447bc9e60c4d223f79fbd
Source noteuspto-grants-2005_11