HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 86678221, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | o-Toluenesulfonyl chloride | HCID 8623 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 71293490 | HCID 71293490 | — |
| Product | HCID 86678221 | HCID 86678221 | — |
Reaction Steps
Intermediate 22 (89 mg, 0.14 mmol) was dissolved in THF (3 ml), and then sodium hydride (6 mg, 0.2 mmol) was added under an atmosphere of N2. The reaction mixture was stirred at RT for 10 mins, then toluenesulfonyl chloride (31 mg, 0.16 mmol) was added and stirring was continued for 16 hours. The reaction mixture was partitioned between EtOAc and water. The organic layer was separated, washed with brine, dried (Na2SO4) and evaporated in vacuo. The resulting residue was purified by silica gel chromatography eluding with a gradient of 50-80% EtOAc in cyclohexane to yield the title compound as a colourless oil (70 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023855B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-7d7921b9083c4fb2a27e6274ff6fc311 |
| Source note | uspto-grants-2015_05 |