HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Benzeneacetyl chloride, 4-bromo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Benzeneacetic acid, 4-bromo- | HCID 74654 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzeneacetyl chloride, 4-bromo- | HCID 181552 | 102.5% |
Reaction Steps
Thionyl chloride (2.5 ml, 34.8 mmol) is added at ambient temperature to a solution of 4-bromophenylacetic acid (Aldrich, 5 g, 23.2 mmol) in 10 ml of toluene. The reaction medium is brought to reflux for 2 hours. After returning to ambient temperature, the toluene is evaporated and 5.55 g of raw 4-bromophenylacetyl chloride is obtained (gross yield=100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265423B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-5d443b11111c4e18a28fb6081c411940 |
| Source note | uspto-grants-2001_07 |