Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (3-Bromophenyl)acetic acid | HCID 74653 | — |
| Product | Ethyl 3-(bromophenyl)acetate | HCID 11470552 | — |
Reaction Steps
Commercially available 2-(3-bromophenyl)acetic acid (13 g 0.06 mol) was dissolved in ethanol (130 ml) and cooled to 0° C. Thionyl chloride (20 ml) was added drop wise. The mixture was heated to 85° C. over night. Reaction mixture was concentrated and the residue was dissolved in ethyl acetate. The organic layer was washed with 10% NaHCO3, water, dried over anhydrous sodium sulfate and concentrated to give 13 g (88%) of A6.1a.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456194B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-6a3d3dfa79a74701a1bb235fef6f8fa9 |
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| Source note | uspto-grants-2008_11 |
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