Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 1-Bromohexadecane | HCID 8213 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (R)-Solketal | HCID 736056 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-O-Hexadecylglycerol | HCID 72733 | 79% |
Reaction Steps
A mixture of 40 ml (R)-(−)-2,2 dimethyl-1,3-dioxolane-4-methanol, 55 grams of powdered potassium hydroxide and 109 ml hexadecyl bromide were added to 500 ml benzene, and the reaction mixture was stirred and refluxed for 6 hours, while removing the water formed by azeotropic distillation. The volume of the solvent was gradually reduced to about 150 ml. The reaction mixture was then cooled to room temperature and stirred at this temperature overnight. Thereafter, 150 ml water was added, and the obtained mixture was extracted thrice with 150 ml diethyl ether. The combined organic phase was washed with 150 ml water and the solvent was then removed under reduced pressure. The residue was dissolved in 200 ml of a mixture of 90:10:5 (volume/volume) methanol:water:concentrated HCl, and the resulting solution was refluxed for 2 hours. After cooling to room temperature and adding 200 ml water, the product was extracted with 250 ml chloroform. The organic phase was washed consecutively with 250 ml water, 200 ml saturated aqueous solution of sodium carbonate, and again with 200 ml water. The solvent was removed under reduced pressure and the product was then crystallized from hexane (500 ml) to give 81.25 grams (yield 79%) of pure 1-hexadecyl-glycerol, which was dried in a desiccator under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999960B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-b5cdd30aff34452692eeeaab88a87680 |
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| Source note | uspto-grants-2015_04 |
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