HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476343Generated: October 30, 2026
Water → (S)-2-hydroxy-N,3-bis(4-hydroxyphenyl)-2-methylpropanamide
https://huagongshe.com/reaction/476343
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | (S)-2-hydroxy-N,3-bis(4-methoxyphenyl)-2-methylpropanamide | HCID 57608122 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-2-hydroxy-N,3-bis(4-hydroxyphenyl)-2-methylpropanamide | HCID 57608124 | 65.6% |
Reaction Steps
(S)-2-hydroxy-N,3-bis(4-methoxyphenyl)-2-methylpropanamide (6c) (0.20 g, 0.63 mmol) was dissolved in dry CH2Cl2 (20 mL). BBr3 (6 mL of 1.0 M CH2Cl2 solution) was added dropwise with stirring via a syringe at room temperature. The reaction solution was allowed to stir overnight at room temperature. The mixture was cooled to 0° C. in a ice bath and hydrolyzed by adding water (25 mL). EtOAc (50 mL) was added to partition the solution. The organic layer was separated; the aqueous layer was extracted with EtOAc (2×10 mL). The organic layers were combined, washed with brine and dried over anhydrous MgSO4. The solvent was removed under vacuum. The residue was purified by flash column chromatography using silica-gel with hexanes/EtOAc (3/7 v/v) to afford a white solid product, (S)-2-hydroxy-N,3-bis(4-hydroxyphenyl)-2-methylpropanamide (6g), 0.12 g, 65.6% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637706B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-c6203fd51f8c41ad9637557b7e7e84ea |
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| Source note | uspto-grants-2014_01 |
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