HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → (4-Fluorophenoxy)acetyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Fluorophenoxyacetic acid | HCID 67882 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (4-Fluorophenoxy)acetyl chloride | HCID 2759057 | 95.4% |
Reaction Steps
Into a 100 ml round bottom flask equipped with a magnetic stirrer, reflux condenser equipped with a connector to a 50% sodium hydroxide trap, 6.81 g (0.040 mole) para-fluorophenoxyacetic acid (the product of Example 2), 2.96 ml (0.044 mole) thionyl chloride, and about 40 ml toluene. The reaction mixture was stirred at reflux for two hours, allowed to cool to room temperature, and then concentrated to give 7.2 g of the product, a brwon liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04479900 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-8c2280aef46a4fe7ab60c4afd38eef12 |
| Source note | uspto-grants-1984_10 |