HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30752Generated: October 28, 2026
Water → 4-Carboxymethoxy-3-ethoxyphenylboronic acid
https://huagongshe.com/reaction/30752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86605505 | HCID 86605505 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Carboxymethoxy-3-ethoxyphenylboronic acid | HCID 23134240 | 64.2% |
Reaction Steps
A 2 mol/L aqueous solution of sodium hydroxide (2.14 mL) was added to a solution of ethyl [2-ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetate (0.15 g) in ethanol (10 mL), and the resulting mixture was stirred at 60° C. for 3 hrs. Water and ethyl acetate were added to the reaction mixture. The aqueous layer was separated, washed with ethyl acetate, made acidic with the addition of 2 mol/L hydrochloric acid, and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford the title compound (0.066 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-9432fbf6457d43c09a8ad818b559f197 |
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| Source note | uspto-grants-2008_09 |
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