HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfate → Methyl 3-methoxy-4,5-dimethyl-2-thiophenecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | Methyl 3-hydroxy-4,5-dimethylthiophene-2-carboxylate | HCID 54691275 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 3-methoxy-4,5-dimethyl-2-thiophenecarboxylate | HCID 14154178 | — |
Reaction Steps
To a solution of methyl 3-hydroxy-4,5-dimethylthiophene-2-carboxylate (Preparation 1) (29.7 g, 160 mmol) in anhydrous acetone (500 ml) was added anhydrous potassium carbonte (24.5 g, 178 mmol) and the mixture stirred for 1 hour at room temperature. Dimethyl sulphate (22.4 g, 178 mmol) was added and the mixture stirred under reflux for 2.5 hours. The solvent was evaporated under reduced pressure and the residue partitioned between water and ethyl acetate. The organic phase was washed with brine, dried with sodium sulphate and evaporated to give crude product which was used in the following preparation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05021449 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-06ce5a78e9424b40aa9393fab3179dce |
| Source note | uspto-grants-1991_06 |