HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenemethanol, 2-ethoxy- → 4-[(2-Ethoxyphenyl)methoxy]-3-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenemethanol, 2-ethoxy- | HCID 51381 | — |
| Reactant | 4-Chloro-3-nitropyridine | HCID 2735781 | — |
| Product | 4-[(2-Ethoxyphenyl)methoxy]-3-nitropyridine | HCID 68699451 | 65.9% |
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 2-ethoxybenzyl alcohol, the titled compound was obtained as a yellow solid. (Yield: 65.9%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07642269B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-f299e3a440e24a7d8759b36c84e7f08c |
| Source note | uspto-grants-2010_01 |