Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86641124 | HCID 86641124 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86641125 | HCID 86641125 | 82% |
Reaction Steps
Compound 35.6 (20 g, 137 mmol) was dissolved in 15 mL dioxane, cooled to 0° C. and treated with 60% NaH (6.0 g, 151 mmol). The mixture was stirred at 0° C. for 30 min and then treated with BnBr (18 mL, 151 mmol). The mixture was warmed to r.t., stirred for 3 h, and then quenched with 50 mL MeOH. The mixture was stirred for another 30 min and the solvent was evaporated under reduced pressure. The residue was subjected to a silica gel column chromatography eluting with 10-50% EtOAc in Hexane to give compound 35.7 (26.55 g, 82% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324179B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-247351ea918c45f7b30edf33cee9f9d2 |
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| Source note | uspto-grants-2012_12 |
|---|