Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Benzeneacetic acid, 4-bromo- | HCID 74654 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzeneacetyl chloride, 4-bromo- | HCID 181552 | — |
Reaction Steps
4-Bromophenylacetic acid (100 g, 0.465 mol), thionyl chloride (300 mL) and DMF (about 2 mL) are charged to a 1-liter round bottom 3-necked flask equipped with a reflux condenser and a mechanical stirrer. The reaction mixture is heated under nitrogen to 50° C. for 2 hours, using a charcoal scrubber for escaping gases. The thionyl chloride is evaporated and the product, 4-bromophenylacetyl chloride, is put into an addition funnel with benzene (30 mL).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06288188B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-8818a3dedc5d48bfb92dcb56d9e98b4d |
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| Source note | uspto-grants-2001_09 |
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