HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromothiophene → 1-(5-Bromothiophen-2-YL)heptan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | Heptanoyl chloride | HCID 17313 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(5-Bromothiophen-2-YL)heptan-1-one | HCID 57675566 | — |
Reaction Steps
2-Bromothiophene (1.63 g, 10.0 mmol) and heptanoyl chloride (1.78 g, 12.0 mmol) were dissolved in dry benzene (15 mL) and AlCl3 was added in portions with stirring over 10 min. The resulting dark brown solution was refluxed for 1 hr and left to cool down to room temperature. The mixture was quenched with 2M HCl (15 mL) carefully while stirred. The organic layer was separated, washed with 2M HCl, 2M NaOH, and water, and passed through silica column (d=3 cm, I=8 cm). The solution was dried over MgSO4, and concentrated in vacuo (2.40 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07528176B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-f2505e8950b24c6d8d33be1cc40a5d5b |
| Source note | uspto-grants-2009_05 |