HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701598Generated: October 26, 2026
m-Chloroperbenzoic acid → 1,2-Di-O-(n-hexadecyl)-3-O-(2,3-epoxypropyl)-glycerol
https://huagongshe.com/reaction/1701598
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1,2-di-O-(n-hexadecyl)-3-allyl-glycerol | HCID 23466103 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1,2-Di-O-(n-hexadecyl)-3-O-(2,3-epoxypropyl)-glycerol | HCID 23466114 | 82% |
Reaction Steps
A solution of 1,2-di-O-(n-hexadecyl)-3-allyl-glycerol (5.8 g., 10.0 mmoles) and m-chloroperbenzoic acid (1.86 g., 10.8 mmoles) in benzene (50 ml.) was stirred at reflux for 16 hours. The reaction mixture was then cooled, treated with saturated aqueous sodium bisulfite solution (10 ml.) and saturated aqueous sodium bicarbonate solution (50 ml.), and extracted with ether (3×50 ml.). The combined ether extract was washed with water (100 ml.), washed with saturated aqueous sodium chloride solution (100 ml.), dried (MgSO4), filtered and evaporated in vacuo to an oil (4.9 g., 82% yield, olefinic protons absent by n.m.r. analysis), which was purified by silica gel chromatography (elution with benzene:ethyl acetate) (4.2 g., 70% yield, oil-solidified on standing).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04193999 |
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| Source dataset | uspto-grants-1980_03 |
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| ORD ID | ord-8ce08193c3494014894cf3f2445edeb7 |
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| Source note | uspto-grants-1980_03 |
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