HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363798Generated: October 30, 2026
1,3-Propanediol → HCID 10951079, compound
https://huagongshe.com/reaction/363798
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | Dibenzo-18-crown-6 | HCID 26541 | — |
| Reactant | HCID 11004225 | HCID 11004225 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10951079 | HCID 10951079 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05874598 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-743cb630b7d24e249b3941834145bfe9 |
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| Source note | uspto-grants-1999_02 |
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