HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl p-toluenesulfonate → 1-Methoxy-2,4-dimethyl-3-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Dimethyl-3-nitrophenol | HCID 13369964 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Methoxy-2,4-dimethyl-3-nitrobenzene | HCID 13369967 | 88.9% |
Reaction Steps
A mixture of 32.12 grams of 2,4-dimethyl-3-nitrophenol, 35.78 grams of methyltosylate and 28.5 grams of anhydrous K2CO3 in 200 ml of acetone is heated to reflux for 12 hours. The reaction mixture is filtered leaving a tan solid. The filtrate is concentrated in vacuo. The concentrated filtrate is taken up in ethyl acetate and extracted with 10% aqueous sodium hydroxide solution and saturated aqueous sodium chloride. The remaining ethyl acetate layer is dried, filtered and concentrated in vacuo to give a dark oil which is distilled (T=80°-87° C./50μ) to give 30.95 grams of a yellow solid which is recrystallized from absolute ethanol, M.P. 53°-55° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04704401 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-2cd6f5f12aea4cbfbca8ec10a9999084 |
| Source note | uspto-grants-1987_11 |