HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Trifluoromethyl)benzenemethanol → 3-Nitro-4-{[4-(trifluoromethyl)phenyl]methoxy}pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Trifluoromethyl)benzenemethanol | HCID 67684 | — |
| Reactant | 4-Chloro-3-nitropyridine | HCID 2735781 | — |
| Product | 3-Nitro-4-{[4-(trifluoromethyl)phenyl]methoxy}pyridine | HCID 68706431 | 89.5% |
Reaction Steps
In accordance with the same procedures as in Preparation 2, except for using 4-chloro-3-nitropyridine prepared in Step 1 of Preparation 1 and 4-trifluoromethylbenzyl alcohol, the titled compound was obtained as a yellow solid. (Yield: 89.5%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07642269B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-09b6b3d025c3449f9d3634eddb89acd4 |
| Source note | uspto-grants-2010_01 |