HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243552Generated: October 26, 2026
Hydrochloric Acid → Ethyl 4'-(2-methanesulfonyloxyethoxy)biphenyl-4-carboxylate
https://huagongshe.com/reaction/2243552
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Ethyl 4'-(2-hydroxyethoxy)biphenyl-4-carboxylate | HCID 23090738 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 4'-(2-methanesulfonyloxyethoxy)biphenyl-4-carboxylate | HCID 23090736 | — |
Reaction Steps
Methanesulfonyl chloride (0.13 mL) was added to an ice-cooled mixture of ethyl 4′-(2-hydroxyethoxy)biphenyl-4-carboxylate (0.41 g) and triethylamine (0.30 mL) in tetra hydrofuran (8 mL) with stirring. The mixture was stirred at that temperature for 30 min, at room temperature for 45 min, and at 45° C. for 1 hr. Methanesulfonyl chloride (0.13 mL) and triethylamine (0.30 mL) were added every an hour to the reaction mixture for 3 times at 45° C., and the mixture was stirred at 70° C. for 3 hrs. 1 mol/L hydrochloric acid and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed with water and brine, and dried over an hydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford ethyl 4′-(2-methanesulfonyloxyethoxy)biphenyl-4-carboxylate (0.32 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674938B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-81292a73c81c427a95e11ce3228c2ff4 |
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| Source note | uspto-grants-2010_03 |
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