HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → HCID 21219136, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | 4-(Trifluoromethyl)benzoyl chloride | HCID 67607 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Catalyst | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21219136 | HCID 21219136 | 84.7% |
Reaction Steps
The title compound was prepared by the procedure described in step 1 of Example 1 using 13.0 g of quinoline, 32.0 g of 4-trifluoromethylbenzoyl chloride, 0.5 g of aluminum chloride, 14.8 g of trimethyl silyl cyanide, and 500 mL of methylene chloride. Crystallization from diethyl ether/hexane afforded the title compound (28.0 g) as a white solid, m. p. 149-151° C. This product was used for the preparation of the title compound described in step 2, and for preparation of the title compound described in Example 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05939435 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-089f8e1579d740e8ab4e0f397dd53d72 |
| Source note | uspto-grants-1999_08 |