HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → HCID 10836187, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 10842123 | HCID 10842123 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10836187 | HCID 10836187 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of the crude ether from Step 5 in THF (10 mL) at 0° C. was added HOAc, (4 drops) followed by n-Bu4NF (1M, THF, 1.4 mL). The reaction mixture was stirred 2 hr at 0° C. then quenched with a saturated solution of NH4Cl and diluted with Et2O. The organic phase was washed with H2O, brine, dried over MgSO4, and the solvent evaporated. The residue was purified by chromatography on silica gel using hexane/EtOAc 7:3 to give the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05227399 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-6e2ebeec14174c2cb0fdf47198c85a8c |
| Source note | uspto-grants-1993_07 |