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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantBoron tribromideHCID 25134—
Reactant(S)-2-hydroxy-N,3-bis(4-methoxyphenyl)-2-methylpropanamideHCID 57608122—
SolventDichloromethaneHCID 6344—
Product(S)-2-hydroxy-N,3-bis(4-hydroxyphenyl)-2-methylpropanamideHCID 5760812465.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637706B2
Source datasetuspto-grants-2014_01
ORD IDord-c6203fd51f8c41ad9637557b7e7e84ea
Source noteuspto-grants-2014_01