Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017033Generated: October 31, 2026

3-Hydroxybenzaldehyde → 3-[[(3-Phenoxyphenyl)amino]methyl]phenol

https://huagongshe.com/reaction/1017033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant3-PhenoxyanilineHCID 77135—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
Product3-[[(3-Phenoxyphenyl)amino]methyl]phenolHCID 1094622769.7%

Reaction Steps

EX-655A) The 3-(phenoxy)aniline (555 mg, 3 mmol) and 3-hydroxybenzaldehyde (366 mg, 3 mmol) were dissolved in 7 mL of 1,2-dichloroethane. Acetic acid (0.189 mL, 3.15 mmol) and solid NaBH(OAc)3 (1.01 g, 5 mmol) were added. The mixture was stirred at room temperature for 3 h, then acidified with 1 N HCl solution. After neutralizing to pH 7.5 with 2.5 N sodium hydroxide, the mixture was extracted with methylene chloride. The organic layer was washed with brine and water, then dried over anhydrous MgSO4, and evaporated to give 609 mg (69%) of the desired N-(3-phenoxyphenyl)[[3-hydroxyphenyl]methyl]amine product as a brown oil, which was greater than 90% pure by reverse phase HPLC analysis. MS m/z=291.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476057B1
Source datasetuspto-grants-2002_11
ORD IDord-7f3c13975c3442f8990b40d48f4d3e8e
Source noteuspto-grants-2002_11