HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → HCID 19791983, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | HCID 19791854 | HCID 19791854 | — |
| Reactant | HCID 178425673 | HCID 178425673 | — |
| Product | HCID 19791983 | HCID 19791983 | — |
Reaction Steps
2-Cyano-4'-methylbenzophenone, prepared as described by G. W. Ebert and R. D. Rieke in J. Organic Chem., 49, 5280-2 (1984), is converted to 5-[2-(4-methylbenzoyl)phenyl]tetrazole by the procedures described in Step 1 of Example 39. Reaction with triphenylmethyl chloride gives N-triphenylmethyl-5-[2-(4-methylbenzoyl)phenyl]tetrazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250548 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-e3427516ac5f460aa63634a210550ef1 |
| Source note | uspto-grants-1993_10 |