HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1-(Methoxymethyl)-3-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22120979 | HCID 22120979 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(Methoxymethyl)-3-nitrobenzene | HCID 11389609 | — |
Reaction Steps
60% Oily sodium hydride (0.22 g, 5.5 mmol) was added to methanol (50 ml) under ice-cooling, and after stirring at room temperature for 30 minutes, 4-[4-(benzyloxy)phenoxy]-3-nitrobenzyl chloride (1.00 g, 2.7 mmol) was added thereto, followed by stirring for 3 hours. The reaction solution was poured into water and extracted with ethyl acetate. After drying, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography [eluent; hexane - chloroform (1:1)] to give 1-[4-benzyloxy)phenoxy]-4-(methoxymethyl)-2-nitrobenzene (0.92 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06156801 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-ce256404ffb34f99a13738da8b2b9ab7 |
| Source note | uspto-grants-2000_12 |