Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Heptane | HCID 8900 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Toluene methylene chloride | HCID 21877217 | — |
| Reactant | HCID 58786211 | HCID 58786211 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58786124 | HCID 58786124 | 17.1% |
Reaction Steps
A 1 M n-heptane solution of boron tribromide (20 ml) was added dropwise to a solution of (1S)-1,5-anhydro-2,3,4,6-tetra-O-benzyl-1-[3-[(3-methylazulen-1-yl)methyl]phenyl]-D-glucitol (0.76 g) in methylene chloride (20 ml) at −78° C. and the mixture was stirred for 30 minutes. Methylene chloride-toluene (ratio: 2:1, 60 ml) was added to the reaction mixture and methanol (6 ml) was further added to the mixture. The reaction mixture was cooled to room temperature and concentrated to the half amount, followed by adding methanol (25 ml) to the mixture and concentrating. This operation was repeated three times. The residue prepared by the concentration was purified by silica gel column chromatography (chloroform-methanol) to obtain (1S)-1,5-anhydro-1-[3-[(3-methylazulen-1-yl)methyl]phenyl]-D-glucitol (0.068 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169761B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-0192b466887c4bd882b2214da1ebae4c |
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| Source note | uspto-grants-2007_01 |
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