HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Ethoxymethyl-2,6-dimethylnitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromomethyl-2,6-dimethylnitrobenzene | HCID 20571860 | — |
| Product | 4-Ethoxymethyl-2,6-dimethylnitrobenzene | HCID 20571865 | — |
Reaction Steps
The product from Step A (19.0 g) is dissolved in ethanol (600 ml) and anhydrous potassium carbonate (32 g) is added. The reaction mixture is stirred at reflux until the reaction is complete by tlc (two hours). The mixture is cooled, and the solids are filtered, washed, and discarded. The filtrate and washings are evaporated to a residue and purified by column chromatography on silica gel, using as eluant cyclohexane/ethyl acetate (97:3 v/v). The desired product, 4-ethoxymethyl-2,6-dimethylnitrobenzene (10.4 g) is isolated as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04287201 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-b7aad892e8e3499c89e4a0223508c013 |
| Source note | uspto-grants-1981_09 |