Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363798Generated: October 30, 2026

1,3-Propanediol → HCID 10951079, compound

https://huagongshe.com/reaction/363798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanediolHCID 10442—
ReactantDibenzo-18-crown-6HCID 26541—
ReactantHCID 11004225HCID 11004225—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
ProductHCID 10951079HCID 1095107972%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 21 mg (5.1×10-5 mol) of 3β,25-dihydroxy-1α,2α-epoxy-5,7-cholestadiene, 294 μl (4.1×10-3 mol) of 1,3-propanediol, 19 mg (1.5×10-4 mol) of potassium t-butoxide and 4.8 mg (1.3×10-5 mol) of dibenzo-18-Crown-6 was stirred in an argon atmosphere at 110° C. (bath temperature) for 4 hours. The reaction mixture was poured into water, and the resulting mixture was extracted twice with ethyl acetate and washed once with a saturated aqueous sodium chloride solution. After drying the ethyl acetate layer over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and the resulting residue was purified by fractional thin layer chromatography (silica gel:dichloromethane:ethanol=100:15) to obtain 18 mg (72% yield) of the titled compound as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874598
Source datasetuspto-grants-1999_02
ORD IDord-743cb630b7d24e249b3941834145bfe9
Source noteuspto-grants-1999_02