HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Bromide → HCID 21521290, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Bromide | HCID 6323 | — |
| Reactant | 1,2,3,4-Tetrahydro-1-methyl-7-propyl-8-quinolinol | HCID 21521308 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21521290 | HCID 21521290 | 76.1% |
Reaction Steps
Into a tube, one introduces 7.5 g of N-methyl-1,2,3,4-tetrahydro-7-propyl-8-hydroxyquinoline (i.e. 0.035 mole) and 4 g of methyl bromide (i.e. 0.035 mole). One adds 10 ml of acetonitrile, one seals the tube and one heats in an oil bath, at 70°C, for 90 hours. After cooling, one dries the compound that is formed, washes with anhydrous ether, and recrystallizes in boiling isopropanol (1 g of product, 2 ml of alcohol). One collects whitish crystals, which one washes again with ether, then one dries the resulting quaternary salt in a drier over sulfuric acid. One obtains 8 g of product, i.e. a yield of 735/1000.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03970454 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-6b9b2b7cdbbd4ce09c2554cfeaba8796 |
| Source note | uspto-grants-1976_07 |