HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl [4'-(2-methanesulfonyloxy-ethoxy)-2',6'-dimethylbiphenyl-4-yloxy]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 86605508 | HCID 86605508 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl [4'-(2-methanesulfonyloxy-ethoxy)-2',6'-dimethylbiphenyl-4-yloxy]acetate | HCID 86605507 | — |
Reaction Steps
Methanesulfonyl chloride (0.17 mL) was added to an ice-cooled mixture of ethyl [4′-(2-hydroxyethoxy)-2′,6′-dimethylbiphenyl-4-yloxy]acetate (0.58 g) and triethylamine (0.36 mL) in methylene chloride (5 mL) with stirring, and the mixture was stirred at room temperature for 1 hr. Water and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford ethyl [4′-(2-methanesulfonyloxyethoxy)-2′,6′-dimethylbiphenyl-4-yloxy]acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07423185B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-3f759c24098a474d8fb6302bb0a88844 |
| Source note | uspto-grants-2008_09 |