HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2,2-Dimethyl-4(5-methyl-thien-2-yl)-chrom-3-en-6-al
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2,2-Dimethyl-4(5-methyl-thien-2-yl)-6-bromo-chrom-3-ene | HCID 86191508 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,2-Dimethyl-4(5-methyl-thien-2-yl)-chrom-3-en-6-al | HCID 131720576 | — |
Reaction Steps
To a cold (−78° C.) solution of 2,2-dimethyl-4(5-methyl-thien-2-yl)-6-bromo-chrom-3-ene (Compound R, 1.2 g, 3.6 mmol) in THF (10 mL), was added t-BuLi in pentane (1.7M solution, 2.3 mL). After 30 minutes, DMF (465 mg, 5 mmol) was added and the mixture was allowed to warm to ambient temperature and stirred for 3 hours. The mixture was diluted with ethyl acetate (150 mL), washed with brine (10 mL), dried and the solvent was removed by evaporation. Purification by chromatography on silica gel column gave the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06538149B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-2cb099e104224a8890bde287ceeb1bf7 |
| Source note | uspto-grants-2003_03 |