HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → 1-methyl-1H-indole-7-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Indole-7-carboxaldehyde | HCID 2734629 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-methyl-1H-indole-7-carbaldehyde | HCID 11040979 | — |
Reaction Steps
A solution of 1H-indole-7-carbaldehyde (500 mg, 3.444 mmol) and dimethylsulfate (478 mg, 3.789 mmol) in DMF (3 ml) was cannulated into a suspension of NaH (99 mg, 95% in mineral oil, 4.133 mmol) in DMF (2 ml) at 0° C. The reaction was stirred and allowed to warmed up to room temperature for 1 hour. The reaction was quenched with water and the product was extracted with EtOAC (×2). The organic layers were combined and washed with water, and brine, and dried (MgSO4) and the solution was concentrated to produce a light pink solid, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193203B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-6274e65efd684335a87e423bcb24230c |
| Source note | uspto-grants-2012_06 |