HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 1-(5-Hydroxy-cyclooctyl)-4-hydroxymethyl-3,3-dimethyl-pyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 131727099 | HCID 131727099 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-Hydroxy-cyclooctyl)-4-hydroxymethyl-3,3-dimethyl-pyrrolidin-2-one | HCID 66665275 | — |
Reaction Steps
Tetrabutyl ammonium fluoride (0.76 mL, 1 M in tetrahydrofuran, 0.76 mmol) was added to a stirred solution of the product of Example 5J (0.30 g, 0.60 mmol) in tetrahydrofuran (5 mL) at room temperature. The resulting solution was stirred for two hours and then partitioned with ethyl acetate and water. The organic phase was washed with brine, dried (MgSO4), filtered, and evaporated. The residue was purified over silica gel using 20-100% ethyl acetate in hexanes to give the titled product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737137B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-8012f60afd3942c4875f0b33cff45857 |
| Source note | uspto-grants-2010_06 |