HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → 3-Bromo-2-[2-(1-trityltetrazol-5-yl)-phenyl]-5-methylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178418484 | HCID 178418484 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-2-[2-(1-trityltetrazol-5-yl)-phenyl]-5-methylbenzofuran | HCID 21848053 | — |
Reaction Steps
5.89 g of triethylamine, 8.14 g of triphenylchloromethane and 0.10 g of 4-N,N-dimethylaminopyridine are added in succession to a suspension of 10.37 g of 3-bromo-2-[2'-(1H-tetrazol-5-yl)-phenyl]-5-methylbenzofuran in 300 ml of CH2Cl2 and the batch is stirred for 3 hours at room temperature. The reaction solution is washed with 150 ml of water and 150 ml of brine, concentrated in vacuo to a volume of 50 ml and chromatographed on silica gel 60 (40-63 μm) using CH2Cl2 as eluant. The product, of Rf =0.82 (CH2Cl2 /CH3OH (95:5)), yields crystalline 3-bromo-2-[2-(1-trityltetrazol-5-yl)-phenyl]-5-methylbenzofuran, m.p. 199-200°, from ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05955487 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-333894c2be5f45d6b900a7e043f1db3f |
| Source note | uspto-grants-1999_09 |