HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30768Generated: October 28, 2026
Water → ethyl (4'-(2-[(1S,2R)-2-hydroxy-2-(4-hydroxyphenyl)-1-methylethylamino]ethoxy}-2',6'-dimethylbiphenyl-4-yloxy)acetate
https://huagongshe.com/reaction/30768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | P-Hydroxynorephedrine | HCID 6931143 | — |
| Reactant | [4'-(2-Methanesulfonyloxyethoxy)-2',6'-di-methylbiphenyl-4-yloxy]acetate | HCID 86605510 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl (4'-(2-[(1S,2R)-2-hydroxy-2-(4-hydroxyphenyl)-1-methylethylamino]ethoxy}-2',6'-dimethylbiphenyl-4-yloxy)acetate | HCID 86605509 | — |
Reaction Steps
A mixture of [4′-(2-methanesulfonyloxyethoxy)-2′,6′-dimethylbiphenyl-4-yloxy]acetate and 4-((1R,2S)-2-amino-1-hydroxypropyl)phenol (0.71 g) in N,N-dimethylformamide (10 mL) was stirred at 80° C. overnight. 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, and the residue was purified by silica gel column chromatography (eluent:methylene chloride/methanol=10/1) to afford ethyl (4′-{2-[(1S,2R)-2-hydroxy-2-(4-hydroxyphenyl)-1-methylethylamino]ethoxy}-2′,6′-dimethylbiphenyl-4-yloxy)acetate (0.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423185B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-b5bd2a4ab78d4cfca8f7ff33c002dd98 |
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| Source note | uspto-grants-2008_09 |
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