Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium azide | HCID 88163 | — |
| Reactant | HCID 18642954 | HCID 18642954 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18642953 | HCID 18642953 | 58% |
Reaction Steps
To a solution of 4.53 g (8.7 mmol) 1-t-butyldimethylsilyloxy-5-benzoyl-3-trifluoromethanesulfonyloxy-2-deoxy-2,2-difluoroxylose in dimethylformamide (50 ml) were added 1.2 g (25.2 mmol) lithium azide and the reaction mixture was heated at 70° C. for 40 minutes. The reaction mixture was then concentrated under reduced pressure and the residue dissolved in ethyl acetate. This solution was washed several times with saturated aqueous sodium chloride, dried over sodium sulfate and concentrated under reduced pressure. The residue was redissolved in a small amount of ethyl acetate and poured over a pad of silica gel, eluting with ethyl acetate. The filtrates were concentrated under reduced pressure to give 2.09 g (58%) of the desired compound as a colorless oil. FD-MS: m/e=356, (M-57, loss of t-butyl), 357((M+1)-57, loss of t-butyl). IR(neat): 2114 cm-1, N3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05644043 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-080b8d7cb99d41679c2ab4a077f8afa9 |
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| Source note | uspto-grants-1997_07 |
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