Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzeneacetic acid, 4-bromo- | HCID 74654 | — |
| Product | Methyl 2-(4-bromophenyl)acetate | HCID 316783 | — |
Reaction Steps
A solution of 202.78 g 4-bromophenylacetic acid in 1.5 L methanol was treated with 15 mL concentrated sulfuric acid and the resulting mixture refluxed under nitrogen for 3 hours. Almost all of the methanol was removed by distillation. Dilute the residue with 1 L ether. Separate the bottom layer and extract that with 2×100 mL ether. Wash the combined ether solution with 3×250 mL 5% NaHCO3 and 250 mL saturated brine, dried over Na2SO4, and concentrated under reduced pressure to give a crude product as light tan oil. Filter that through 300 g silica gel with 10% EtOAc in hexanes and concentrated under reduced pressure to give the title compound as colorless oil. 1H NMR (CDCl3, 500 MHz) δ 7.46˜7.48 (m, 2H), 7.16˜7.19 (m, 2H), 3.72 (s, 3H), 3.60 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989475B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-cd0dc33ef1cd46feab8ce5dd649e9ad6 |
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| Source note | uspto-grants-2011_08 |
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