Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Phenyl 3,4-di-O-acetyl-2-O-benzyl-6-deoxy-1-thio-alpha-L-mannopyranoside | HCID 46782732 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11463747 | HCID 11463747 | — |
Reaction Steps
To a solution containing 1.00 g (2.32 mmol) of 8 in 25 mL of anhydrous CH2Cl2 at 0° C. under argon was added 0.50 g (0.16 mL, 3.14 mmol) of Br2. The reaction mixture was stirred at 0° C. for 1 h. The reaction mixture was diluted with 20 mL of CH2Cl2 and washed with 100 mL of 3% aq NaHSO3. The organic layer was separated, dried (MgSO4) and concentrated under diminished pressure. The residue was then purified by flash chromatography on a silica gel column (26×4 cm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605241B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-cba4be8a96eb429f865275fa42852db2 |
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| Source note | uspto-grants-2009_10 |
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