HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2,2-Dimethyl-4(2-methyl-thien-5-yl)-thiochrom-3-en-6-al
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2,2-Dimethyl-4(2-methyl-thien-5-yl)-6-bromo-thiochrom-3-ene | HCID 86191489 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,2-Dimethyl-4(2-methyl-thien-5-yl)-thiochrom-3-en-6-al | HCID 131720577 | — |
Reaction Steps
To a cold (-78° C.) solution of 2,2-dimethyl-4(2-methyl-thien-5-yl)-6-bromo-thiochrom-3-ene (Compound T, 430 mg, 1.2 mmol) in THF (12 mL) was added n-BuLi in hexane (1.6M solution, 1 mL). The mixture was gradually warmed to ambient temperature over 1 hour and recooled to -78° C. To this solution was added DMF (220 mg, 3 mmol) and the mixture was stirred at ambient temperature for 16 hours. The reaction was quenched by adding water (10 mL) and ethy lacetate (100 mL). The organic layer was washed with brine (10 mL), dried and the solvent was removed by distillation to obtain the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728846 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-cd5084750b36490791be0dc4f9686048 |
| Source note | uspto-grants-1998_03 |