HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058651Generated: October 27, 2026
Hexane → 3-(4-Chlorobenzoyl)-2-(4-chlorophenylthio)-5-dimethoxymethylthiophene
https://huagongshe.com/reaction/1058651
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Chloro-N-methoxy-N-methylbenzamide | HCID 11275663 | — |
| Reactant | 3-Bromo-2-(4-chlorophenylthio)-5-dimethoxymethylthiophene | HCID 18668927 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Chlorobenzoyl)-2-(4-chlorophenylthio)-5-dimethoxymethylthiophene | HCID 18669009 | 60% |
Reaction Steps
In an argon atmosphere, 3-bromo-2-(4-chlorophenylthio)-5-dimethoxymethylthiophene (500 mg, 1.32 mmol) obtained in Example 90 was dissolved in tetrahydrofuran (6 mL) and cooled to −78° C. n-Butyl lithium (a 1.6 mol/L hexane solution, 0.81 mL, 1.3 mmol) and tetrahydrofuran (1 mL) solution of 4-chloro-N-methoxy-N-methylbenzamide (528 mg, 2.64 mmol) were added thereto, followed by stirring for 10 minutes. Water was added to the reaction liquid and the product was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (15:1 hexane/ethyl acetate) to give 3-(4-chlorobenzoyl)-2-(4-chlorophenylthio)-5-dimethoxymethylthiophene (345 mg, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518268B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-8bf48d9fca4f4237899c4e137fe698a0 |
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| Source note | uspto-grants-2003_02 |
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