HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzophenone → 2(1-Methyltetrazol-5-yl)-1,1-diphenylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | 1,5-Dimethyltetrazole | HCID 78825 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2(1-Methyltetrazol-5-yl)-1,1-diphenylethanol | HCID 14724036 | 22% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
A solution of 1,5-dimethyltetrazole (20 g; 0.204 mole) in dry THF (200 mL) was cooled to -78° C. and treated with n-butyllithium (91 mL of 2.5 molar solution in hexane; 0.227 mole) and the mixture stirred at -78° C. for 30 minutes. Benzophenone (31.1 g; 0.171 mole) was added and the mixture stirred at -78° C. for 30 minutes and allowed to warm up to 23° C. and stirred for 15 hours. The mixture was quenched with 2N HCl (100 mL) and extracted with EtOAc (3×150 mL). The combined organic layers were dried (MgSO4) and evaporated. The residue was crystallized from EtOAc-Hexane to afford the title compound as a white solid (10.5 g; 22%); m.p.=175°-176° C. (crystallized from EtOAc-hexane). MS (CI): m/e=281 for (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05110940 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-4b1e4e7f20a04934a64030117cf3c3fc |
| Source note | uspto-grants-1992_05 |