HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701595Generated: October 25, 2026
Allyl bromide → 1,2-di-O-(n-hexadecyl)-3-allyl-glycerol
https://huagongshe.com/reaction/1701595
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,3-Bis(hexadecyloxy)propan-1-ol | HCID 102548 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,2-di-O-(n-hexadecyl)-3-allyl-glycerol | HCID 23466103 | 93% |
Reaction Steps
Sodium hydride (1.78 g. of 50 wt. % dispersion in mineral oil, 37 mmoles) was added at 60° C. to a solution of 1,2-di-O-(n-hexadecyl)-glycerol (10 g., 18.5 mmoles) in N,N-dimethylformamide (100 ml.), and the resulting solution stirred for 20 minutes at 60° C. Allyl bromide (4.47 g., 37 mmoles) was then added dropwise and the resulting mixture stirred for 3 hours at 90° C., cooled, cautiosly diluted with water (200 ml.) to quench the reaction, and extracted with ether (3×150 ml.). The combined ether extract was washed with saturated aqueous sodium chloride solution, dried (MgSO4), filtered and evaporated in vacuo to an oil, which was purified by silica gel chromatography (elution with benzene) [10 g., 93% yield, oil, n.m.r. (CDCl3) δ 5.66-6.16 (m, 1, --OCH2CH=CH2), 5.25 (d of doublets, 2, --OCH2CH=CH2) and 4.03 (d, 2, --OCH2CH=CH2)].
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-ab42812d146c4f84a092492634ec97f7 |
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| Source note | uspto-grants-1980_03 |
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