Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | L-(-)-Sorbose | HCID 6904 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Product | Diacetone L-sorbose | HCID 11043496 | 58.4% |
Reaction Steps
To 200 ml of acetone were added 10.0 g of L-sorbose and 225 mg of N-iodosuccinimide and the mixture was refluxed with stirring in a water bath at 60° C. for 6 hours. During this reaction, the refluxing solvent was dried with 20 g of Molecular Sieves 3A interposed between the reaction vessel and the cooling jacket. The reaction mixture was then subjected to an after-treatment similar to that described in Example 11 to give 8.43 g (58.4%) of 2,3:4,6-di-O-isopropylidene-L-sorbofuranose (purity ≥97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04464530 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-e9eb00c953be4be9ae291df8ab30e400 |
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| Source note | uspto-grants-1984_08 |
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