Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 3-Bromo-2,5-dichlorothiophene | HCID 521925 | — |
| Reactant | [3,5-Bis(methoxycarbonyl)phenyl]boronic acid | HCID 19363104 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21838297 | HCID 21838297 | 58.2% |
Reaction Steps
A mixture of 3-bromo-2,5-dichlorothiophene (0.30 g), [3,5-bis(methoxycarbonyl)phenyl]-dihydroxyborane (0.37 g), lithium chloride (0.164 g), tetrakis(triphenylphosphine)palladium(0) (0.0747 g) and 2M aqueous sodium carbonate solution (1.55 ml) in 1,2-dimethoxyethane (3.6 ml) was heated at 85° C. and stirred vigorously for 4 hours under nitrogen. The reaction mixture was cooled to room temperature and to the mixture was added ethyl acetate (20 ml) and 2M sodium carbonate solution (20 ml). The layers were separated, and the organic layer was washed successively with water and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel eluting with a mixture of hexane and ethyl acetate (20:1). The fractions containing the desired product were collected and evaporated in vacuo to give dimethyl 5-(2,5-dichlorothiophen-3-yl)isophthalate (0.26 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05968985 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-f1f2b81f1a144d5b929c69cf4ab2d083 |
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| Source note | uspto-grants-1999_10 |
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