Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sucrose | HCID 5988 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57476952 | HCID 57476952 | — |
Reaction Steps
96 g of ion exchange water and 96 g (2.4 moles) of sodium hydroxide were added to a 1 L four-necked separable flask equipped with a stirrer, a reflux condenser and a dropping funnel to dissolve the sodium hydroxide in the ion exchange water. 68.4 g (0.2 moles) of sucrose was further added, and reacted at 80° C. for 90 minutes while stirring to obtain an alkaline sucrose aqueous solution. 290 g (2.4 moles) of allyl bromide was added dropwise into the alkaline sucrose aqueous solution for 2 hours while controlling rapid heating caused by an etherification reaction. Thereafter, the etherification reaction was completed by aging the reaction solution at 80° C. for 3 hours. After cooling, 400 g of ion exchange water was added to the reaction solution taken from the separable flask, and unwanted water-soluble components were removed from the oils to obtain crude oil-soluble sucrose allyl ether. Subsequently, 250 g of ion exchange water was added, and volatile components formed as the by-products were distilled off together with water using a rotary evaporator. 120 g of n-hexane and 40 g of ion exchange water were further added, and water-soluble impurities were removed again through liquid separation. The n-hexane was distilled off from the separated oily phase using a rotary evaporator to obtain 110 g of purified oil-soluble sucrose allyl ether. The etherification degree of the oil-soluble sucrose allyl ether was 6.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139671B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-532a274e18f149978a5998eb45bba17c |
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| Source note | uspto-grants-2015_09 |
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