HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(Methylcarbonyloxy)phenethyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Benzeneethanol, 4-(acetyloxy)- | HCID 586676 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Methylcarbonyloxy)phenethyl methanesulfonate | HCID 21704989 | 97.2% |
Reaction Steps
55 g (0.305 mole) 2-(4-methylcarbonyloxyphenyl)-1-ethanol and 34.4 g (0.341 mole) triethylamine in 300 ml dichloromethane were cooled on an ice bath. 38.5 g (0.336 mole) methanesulfonyl chloride was slowly added. The ice bath was removed and the mixture was stirred for 3 hours at room temperature. Water was added and the phases were separated. The organic phase was washed with saturated sodium hydrogen bicarbonate and brine, dried (magnesium sulfate), filtered and evaporated in vacuo to give 76.6 g (yield 97%) of 4-(methylcarbonyloxy)phenethyl methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06288096B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-ebd58084eae847f7b137bb1746131eae |
| Source note | uspto-grants-2001_09 |