HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3-methylbutane → 4-(3-Methylbutoxy)-2-nitrotoluene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3-methylbutane | HCID 7891 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Nitro-p-cresol | HCID 16271 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(3-Methylbutoxy)-2-nitrotoluene | HCID 21545969 | — |
Reaction Steps
A mixture of 50 parts of 3-nitro-p-cresol, 94 parts of isoamyl bromide and 94.2 parts of anhydrous potassium carbonate in 650 parts of acetone was stirred and heated under reflux for 18 hours. Insoluble material was filtered off and washed with acetone and the total acetone solution was evaporated. An oil remained which was partitioned between 250 parts of ether and 500 parts of water. The ethereal layer was isolated dried over anhydrous magnesium sulphate then evaporated to leave 66.6 parts of 4-(3-methylbutoxy)-2-nitrotoluene as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03952013 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-fa653e091d1a4f149fbf1e25c83f77cf |
| Source note | uspto-grants-1976_04 |