Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 17993053 | HCID 17993053 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59303954 | HCID 59303954 | — |
Reaction Steps
3-Butoxymethylthiophene (6.17 grams, 36.24 mmol) was dissolved in 100 milliliters of CH2Cl2, and then 100 milliliters of acetic acid (AcOH) were added. N-Bromosuccinimide (NBS) (6.45 grams, 36.24 mmol) was then added in portions to the resulting mixture under stirring. The mixture resulting was then stirred at room temperature, about 23° C. to about 27° C., for 24 hours. Reaction completion was determined by 1H NMR. The solvents were then removed by evacuation. The residue remaining was dissolved in hexane, and the soluble part was passed through a short silica gel column (10 centimeters×3 centimeters). After removing the solvent, the resulting colorless liquid was purified by column chromatography using hexane/CH2CI2 (3/2, v/v) then by distillation under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718999B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-aabdb25faee34766b22ffc1dda43a448 |
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| Source note | uspto-grants-2010_05 |
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