Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | HCID 22882479 | HCID 22882479 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22882478 | HCID 22882478 | — |
Reaction Steps
15.1 g of 3-tert-butoxycarbonyl-2,2-dimethyl-4(S)-[1-(2-hydroxyethyl)cyclopropylmethyl]-1,3-oxazolidine are dissolved in 50 ml of tetrahydrofuran, and 14.2 g of a potassium hydride suspension (20% in oil) are added at 0° C. The mixture is stirred at 0° C. for 1 h and 6.3 ml of benzyl bromide are then added dropwise, while stirring. After 90 min., 100 ml of water are slowly added to the reaction mixture and the aqueous phase is extracted with diethyl ether. This gives the title compound: Rf (A)=0.8; FAB-MS: (M+H)+ =390.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05719141 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-e2d3c66da1ce4034b1d41d6654284c16 |
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| Source note | uspto-grants-1998_02 |
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