HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → (4-Chloro-2-hydroxyphenoxy)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | 2-(4-Chloro-2-methoxyphenoxy)acetic acid | HCID 11658584 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-Chloro-2-hydroxyphenoxy)acetic acid | HCID 16748825 | — |
Reaction Steps
To a solution of 48% aqueous hyrdrogen bromide (20 mL) was added (4-chloro-2-methoxy-phenoxy)-acetic acid (2.1 g, 9.7 mmol). The resulting mixture was heated to reflux overnight. The mixture was cooled to ambient temperature, diluted with water and extracted with diethyl ether. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo to give (4-chloro-2-hydroxy-phenoxy)-acetic acid. The crude product was added to a solution of pyridinium p-toluene sulfonate (0.10 g, 0.40 mmol) in toluene (100 mL). The resulting mixture was heated to reflux for five hours. The reaction was allowed to cool to ambient temperature and concentrated in vacuo. Chromatography on silica gel gave the title compound (0.97 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07098212B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-a62f0d2dcbcb40f2a0c77212a8c65747 |
| Source note | uspto-grants-2006_08 |