Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzyl bromide | HCID 122573 | — |
| Reactant | HCID 18464680 | HCID 18464680 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 22009080 | HCID 22009080 | — |
Reaction Steps
Combine 1-(3,4,5-trimethoxybenzyl)-3-(2-(t-butyldimethylsilyloxy)ethyl)-2-oxopyrrolidine (0.31 g, 0.74 mmol) and tetrahydrofuran (2 mL). Cool to −78° C. using a dry-ice/acetone bath. Add a solution of sec-butyllithium (0.63 mL, 1.3 M in hexane, 0.81 mmol). After 30 minutes, add a solution of 3,5-di(trifluoromethyl)benzyl bromide (0.25 g, 0.81 mmol) in tetrahydrofuran (1 mL). After 2 hours, warm to ambient temperature. After 12 hours, add water (10 mL). Separate the layers and extract the aqueous layer three times with ethyl acetate. Dry the combined organic layers over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 1/4 ethyl acetate/hexane to give the title compound: Rf=0.44 (silica gel, 1/4 ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211199B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-9dc6ef72b0684b4e9371b02f4097a1fe |
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| Source note | uspto-grants-2001_04 |
|---|