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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361007Generated: October 25, 2026

P-Anisidine → 2-Hydroxy-5-[(4-methoxyphenylamino)methyl]benzoic Acid

https://huagongshe.com/reaction/1361007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantEthyl AcetateHCID 8857—
Reactant5-Formylsalicylic acidHCID 69226—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-Hydroxy-5-[(4-methoxyphenylamino)methyl]benzoic AcidHCID 57457041—

Reaction Steps

p-Anisidine (1.3 g, 10.6 mmol) was dissolved in methanol (20 mL) and 5-formylsalicylic acid (1.75 g, 10.6 mmol) was added and the resulting mixture was stirred at room temperature for 16 hours. The solid formed was isolated by filtration, re-dissolved in N-methyl pyrrolidone (20 mL) and methanol (2 mL). To the mixture was added sodium cyanoborohydride (1.2 g) and the mixture was heated to 70° C. for 3 hours. To the cooled mixture was added ethyl acetate (100 mL) and the mixture was extracted with water (100 mL) and saturated aqueous ammonium chloride (100 mL). The combined aqueous phases were concentrated in vacuo and a 2 g aliquot was purified by SepPac chromatography eluting with mixtures of aetonitrile and water containing 0.1% trifluoroacetic acid to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879893B2
Source datasetuspto-grants-2011_02
ORD IDord-c72f71c63c074a2a9a6e5f80193b0f05
Source noteuspto-grants-2011_02