HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 67005800, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethane, azido- | HCID 79118 | — |
| Reactant | HCID 59252753 | HCID 59252753 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67005800 | HCID 67005800 | — |
Reaction Steps
To a solution of (1H-indazol-5-yl)(phenyl)methanol (1.1 g, 5.0 mmol) in 50 mL of dry THF was added EtN3 (2.8 mL, 20 mmol) and acetic anhydride (1.9 mL, 20 mmol). The reaction was heated at reflux for 12 h. The reaction was quenched with aqueous sodium bicarbonate and extracted 2×EtOAc. The organic layers were dried over MgSO4, filtered, and concentrated. The residue was taken up in toluene and concentrated in vacuo×2 to remove any excess acetic anhydride. Obtained a quantitative yield of (1H-indazol-5-yl)(phenyl)methyl acetate. MS found: (M+H)+=309.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08067447B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-f191b46d9b794ff7b0905c440f0648a4 |
| Source note | uspto-grants-2011_11 |