HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → 5-phenyl-1-trityl-1H-tetrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178418369 | HCID 178418369 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-phenyl-1-trityl-1H-tetrazole | HCID 10430358 | 94.1% |
Reaction Steps
A solution of 5-phenyl-1H-tetrazole (50.0 g, 342.1 mmol, 1.00 equiv) in DCM (dried) (150 mL) was placed in a flask that had been purged and maintained with an inert atmosphere of nitrogen. Triethylamine (45.0 g, 444.7 mmol, 1.30 equiv) at 0° C. was added to the mixture, followed by the addition of chlorotriphenylmethane (100.0 g, 358.7 mmol, 1.05 equiv) in several batches at 0° C. The resulting solution was stirred for 3 hours at room temperature. The solids were collected by filtration, and the filtrate cake was washed with cold EtOAc (1×100 mL) and water (3×300 mL). The solid was dried under reduced pressure to yield 125 g (94%) of 5-phenyl-1-trityl-1H-tetrazole as a white solid. ES m/z: [M+H]+ calcd for C26H20N4, 389.1. found 389.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08865755B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-1a49ea5e26c34a65b4f2c2e24f0c3a20 |
| Source note | uspto-grants-2014_10 |