HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-(Dimethoxymethyl)thiophene-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-(Dimethoxymethyl)thiophene | HCID 15918138 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Dimethoxymethyl)thiophene-2-carbaldehyde | HCID 15918139 | 80% |
Reaction Steps
To a solution of 3-dimethoxymethylthiophene (14 g) in tetrahydrofuran (80 ml) was slowly added n-butyllithium (1.6M in n-hexane, 47.8 ml) at -10° C. with stirring. The reaction mixture was further stirred at same temperature for 1 hour. N,N-Dimethyl-formamide (11.9 g) in tetrahydrofuran (40 ml) was then added. The reaction mixture was warmed to room temperature and stirred for overnight. Ice water was added and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated to give brownish oily product (13 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05741811 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-53ea99193a3e4c8788b97e39e03f7dba |
| Source note | uspto-grants-1998_04 |