HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoacetic Acid → (2,3-Dichloro-4-acryloylphenoxy)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoacetic Acid | HCID 5240 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Dichloro-4-acryloylphenol | HCID 13958744 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (2,3-Dichloro-4-acryloylphenoxy)-acetic acid | HCID 13958742 | 35.7% |
Reaction Steps
2,3-Dichloro-4-acryloylphenol (4.85 g, 0.0224 mole), iodoacetic acid (4.5 g, 0.24 mole), potassium carbonate (3.33 g, 0.024 mole) and acetone (200 ml) were united, stirred and refluxed for 20 hours. The reaction mixture was cooled and the solid removed by filtration, dissolved in water (100 ml) and acidified to a pH of 1 with concentrated hydrochloric acid. The material that separated was extracted with chloroform, the organic layer removed, washed with water, dried over MgSO4, filtered and the solvent removed by evaporation in vacuo. The residue was recrystallized from carbon tetrachloride to give 2.2 g of (2,3-dichloro-4-acryloylphenoxy)-acetic acid, m.p. 111°-113° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04699926 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-e78cce5e0b18492bb04bdc49b63ef128 |
| Source note | uspto-grants-1987_10 |