Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | L-(-)-Sorbose | HCID 6904 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Diacetone L-sorbose | HCID 11043496 | 152.3% |
Reaction Steps
To 200 ml of acetone were added 10.0 g of L-sorbose, 143 mg of cuprous oxide and 173 mg of 47% hydrobromic acid, and the mixture was refluxed in a warm-water bath at 60° C. for 8 hours. The refluxing solvent was continuously dried with 20 g of molecular sieves 3A which was placed between the reaction vessel and the cooling tube. After the conclusion of the reaction, the same post-treatment as in Example 5 was carried out, thus giving 11.0 g (76.2%) of 2,3:4,6-di-O-isopropylidene-L-sorbofuranose.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04460767 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-a167d522cdb949d3a16b23eca94a0f03 |
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| Source note | uspto-grants-1984_07 |
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