HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-Phenylbenzo[b]thiophene-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-Phenylbenzothiophene | HCID 610881 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Phenylbenzo[b]thiophene-2-carbaldehyde | HCID 10514100 | — |
Reaction Conditions
| Temperature | -70 °C |
|---|
Reaction Steps
Butyllithium (62.5 ml of 1.6M solution in hexane, 0.1 mole) was added dropwise to a stirred solution of 3-phenylbenzo[b]thiophene (21.0 g, 0.1 mole) in tetrahydrofuran (150 ml) at -70° C. The solution was stirred at -70° C. for 30 minutes and dimethylformamide (10 ml, 0.13 mole) was added. The resulting mixture was stirred at -70° C. for 30 minutes and then allowed to warm to ambient temperature. After a further hour the reaction was quenched by the addition of dilute hydrochloric acid (100 ml, 2M) and the tetrahydrofuran removed under reduced pressure. The resulting oil was extracted into diethyl ether, the ethereal extract washed with water, dried over potassium carbonate and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04654352 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-6ab892673fc045028a5497921f9c43ee |
| Source note | uspto-grants-1987_03 |