HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Ethyl 1-methyl-1-(4-methylphenyl)ethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl 4-methylphenylmethanesulfonate | HCID 12456502 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | Ethyl 1-methyl-1-(4-methylphenyl)ethanesulfonate | HCID 21706484 | 77% |
Reaction Conditions
| Temperature | -40 °C |
|---|
Reaction Steps
To a solution of butyllithium (2.5M in hexanes, 2.94 mL) in THF (3.5 mL) cooled to −60° C. was added ethyl 4-methylphenylmethanesulfonate (1.05 g, 4.91 mmol) in THF (5 mL). After 15 minutes, iodomethane (0.61 mL, 9.8 mmol) was added, and the mixture was stirred for 1 hour at −50 to −30° C. The mixture was recooled to −60° C., and further butyllithium (2.94 mL) and iodomethane (0.61 mL) were added. The reaction was quenched with aqueous ammonium chloride, and extracted with ether. The organic phase was dried (K2CO3), filtered and evaporated. Chromatography of the residue over silica gel (15% ethyl acetate/hexane) gave ethyl 1-methyl-1-(4-methylphenyl)ethanesulfonate (0.917 g, 3.79 mmol, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06268365B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-9df3ae5750264a0fb0df3355a01795fc |
| Source note | uspto-grants-2001_07 |