Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | HCID 54258721 | HCID 54258721 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54005197 | HCID 54005197 | — |
Reaction Steps
A mixture of 1.07 g (2.69 mmol) of 5-[[2-(2-ethoxy-2-oxoethyl)phenyl]carbonyl]-2-methoxybenzenepropanoic acid ethyl ester and 3.63 g (31.41 mmol) of pyridine hydrochloride was heated at 220°-260° C. for 40 min and then cooled to room temperature. Aqueous 3N sulfuric acid (40 mL) was added, and the mixture was worked-up with ethyl acetate in the usual manner. The crude product was dissolved in 150 mL of ethanol. To this solution was added 3 mL of thionyl chloride and the resulting solution was heated at reflux for 16 hr. The solvent was removed in vacuo and the crude product was purified by flash chromatography on 120 g of silica gel, eluting with 3:1 hexane-ethyl acetate. This afforded 0.469 g (45.4%) of the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05273999 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-531b3a0cbfe848e8a4e4b7744d38f375 |
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| Source note | uspto-grants-1993_12 |
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