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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595528Generated: October 26, 2026

Water → Methyl 3alpha,7alpha-ditetrahydropyranyloxy-5beta-cholan-24-oate

https://huagongshe.com/reaction/595528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantMethyl chenodeoxycholateHCID 11069533—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3alpha,7alpha-ditetrahydropyranyloxy-5beta-cholan-24-oateHCID 6673765890%

Reaction Steps

p-Toluenesulfonic acid (78 mg, 0.41 mmol), 3,4-dihydro-2H-pyrane (20.1 ml, 0.098 mol) were added to a solution of methyl 3α,7α-dihydroxy-5β-cholan-24-oate (1) (2.0 g, 4.9 mmol) in dioxane (6 mL). The reaction mixture was stirred at room temperature for 15 min. H2O (50 mL) was then added and the mixture was partially concentrated under vacuum and extracted with EtOAc (3×50 mL). The combined organic fractions were washed with brine (1×50 mL), dried (Na2SO4) and evaporated under vacuum. The residue was purified by chromatography on silica gel column. Elution with light petroleum/ethyl acetate 80/20 afforded 2.5 g of the pure compound 2 (90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09243027B2
Source datasetuspto-grants-2016_01
ORD IDord-f98b4d82b9b345829cc15626469c0a7c
Source noteuspto-grants-2016_01