HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → HCID 67206080, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 69233329 | HCID 69233329 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67206080 | HCID 67206080 | 39.1% |
Reaction Steps
To a solution of (3R)-6-Fluoro-2,3,4,9-tetrahydro-1H-carbazole-3-carboxylic acid (0.60 g, 2.57 mmol) in anhydrous 1,4-dioxane (20 mL) was added diphenylphosphorylazide (0.7 mL, 3.24 mmol), triethylamine (0.39 mL, 2.83 mmol), and 4 A molecular sieves. After stirring at room temperature for 2 h, benzyl alcohol (0.8 mL, 7.71 mmol) was added and the reaction was heated at 70° C. for 2 h. After cooling, the mixture was filtered and the filtrate was concentrated in vacuo. Purification by chromatography on silica gel afforded 340 mg of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07297704B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-b77da451bda945abbc8abcc97044b55a |
| Source note | uspto-grants-2007_11 |