HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → HCID 10717786, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178467510 | HCID 178467510 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10717786 | HCID 10717786 | 100.5% |
Reaction Steps
3-(3-Ethoxy-4-methylisoxazol-5-yl)-1H-1,2,4-triazole (1.1 g, 5.7 mmol), triethylamine (2.5 mL, 18 mmol) and DMF (20 mL) was added trityl chloride (1.6 g, 5.7 mmol) in DMF (5 mL). The mixture was stirred at room temperature for 5 h and poured onto an ice/water mixture (200 mL). The aqueous phase was extracted with diethyl ether (3×200 mL) and the organic extracts were washed with an aqueous solution of Na2CO3 (10%) (200 mL) and brine (200 mL). The solution was dried (Na2SO4) and concentrated in vacuo to give crude title compound (2.5 g). A small sample was crystallized (EtOAc) to give a single isomer as colourless crystals: mp 181-183° C. The crude product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06200999B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-545c402417134d8a9fbfdd9935256604 |
| Source note | uspto-grants-2001_03 |