HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 4-Octyloxy-3-bromobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Bromo-4 octyloxybenzoic acid chloride | HCID 19847001 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-Octyloxy-3-bromobenzoic acid | HCID 23333447 | — |
Reaction Steps
540 mg (≃0.002 mole) of ##STR17## C5H11 and 700 mg (≃0.002 mole) of 3-bromo-4 octyloxybenzoic acid chloride are charged in a reactor containing 10 ml of pyridine and kept at ambient temperature for 48 hours. The reaction mixture is then poured into a solution containing 10 ml of concentrated H2SO4 and 100 g of ice. The organic fraction is extracted three times with ether then washed three times with water and finally dried on anhydrous Na2SO4. The solvent is evaporated and the product is recrystallised three times in ethanol. 850 ml of product are obtained. The molar efficiency is 73%. Step (d) of substituting the cyanide group for the bromine group
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04222888 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-0817aa66841f4e4ea1624ceb904cd90c |
| Source note | uspto-grants-1980_09 |