HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-(4-Methoxy-benzenesulfonyl)-2-methyl-3-phenyl-propionic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 2-(4-Methoxy-benzenesulfonyl)-3-phenyl-propionic acid ethyl ester | HCID 10893429 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(4-Methoxy-benzenesulfonyl)-2-methyl-3-phenyl-propionic acid ethyl ester | HCID 10948439 | — |
Reaction Steps
To a stirred solution of 2-(4-methoxy-benzenesulfonyl)-3-phenyl-propionic acid ethyl ester (1.0 gm, 3 mmol) (example 9), methyl iodide (1 ml, excess) and 18-Crown-6 (500 mg) in acetone (250 ml), K2CO3 (10 gm, excess) was added and the reaction mixture was refluxed for 24 hours. At the end, the reaction mixture was filtered and the acetone layer was concentrated. The residue obtained was extracted with chloroform, washed well with water, dried over anhydrous MgSO4, filtered and concentrated. The product obtained was purified by silica-gel column chromatography by eluting it with 30% ethyl acetate:hexanes to afford 2-(4-methoxy-benzenesulfonyl)-2-methyl-3-phenyl-propionic acid ethyl ester as a colorless oil. Yield 1.0 g, 98%; MS: 349 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06462073B2 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-b6fa46a62ef24cbeb4136206f8b50101 |
| Source note | uspto-grants-2002_10 |