HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → p-Toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxy-4-methylbenzaldehyde | HCID 61200 | — |
| Reactant | 3-Methoxypropyl 4-methylbenzenesulfonate | HCID 13522988 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | p-Toluenesulfonate | HCID 85570 | 30% |
| Product | 2-(3-Methoxypropoxy)-4-methylbenzaldehyde | HCID 86053432 | — |
Reaction Steps
A solution of 2-hydroxy-4-methylbenzaldehyde (3 g, 21.6 mmol), potassium carbonate (14.9 g, 107.8 mmol) and the title A compound, toluene-4-sulfonic acid 3-methoxy-propyl ester (8.07 g, 32.4 mmol) in DMF (50 mL) is stirred at 50° C. for 3 h. The solvent is concentrated under reduced pressure, H2O is added, and the aqueous layer extracted twice with ethyl acetate. The combined organic extracts are dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the title compound together with 30% of remaining tosylate: Rt (HPLC, Nucleosil C18, 10:90-100:0 CH3CN/H2O+0.1% TFA within 5 min, then 100% CH3CN+0.1% TFA): 5.25, 5.39 min. The mixture is further used as is in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754727B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-004cb6297a034d938bb925bac4cb8f92 |
| Source note | uspto-grants-2010_07 |