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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957934Generated: October 26, 2026

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

https://huagongshe.com/reaction/1957934

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 numberUS08410083B2
Source datasetuspto-grants-2013_04
ORD IDord-e984c97df48947a3b63eb7d7b801d606
Source noteuspto-grants-2013_04