HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5-Bromonaphthalene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | 1-Naphthoic acid | HCID 6847 | — |
| Reactant | Bromine | HCID 24408 | — |
| Catalyst | Bromine | HCID 24408 | — |
| Product | 5-Bromonaphthalene-2-carboxylic acid | HCID 14960646 | — |
Reaction Steps
To naphthoic acid (50 g) (ex Aldrich) in glacial acetic acid at reflux was added a few drops of bromine (ex BDH) followed by iodine (0.5 g) (ex (BDH). Bromine (15 ml) was added dropwise over one hour. The mixture was cooled to 25° and stirred there for 18 hours. The resulting white precipitate was filtered, dissolved in hot water and treated with concentrated hydrochloric acid. The precipitate was filtered and dried (over phosphorus pentoxide (ex BDH) to give 5-bromo-2-napthoic acid (recrystallised from ethanol) (28 g). Melting point 261°-2°. NMR 1H:(DMSO,CDCl3), 8.60(1H,s), 8.00(5H,m), 7.40(1H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05202356 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-349a6dae78c1414ca5a23eea3348f7bb |
| Source note | uspto-grants-1993_04 |