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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18441Generated: October 27, 2026

4-Bromobenzaldehyde → 4-(4-Bromo-benzylamino)-2-hydroxy-benzoic acid methyl ester

https://huagongshe.com/reaction/18441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzaldehydeHCID 70741—
ReactantMethyl p-aminosalicylateHCID 77787—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product4-(4-Bromo-benzylamino)-2-hydroxy-benzoic acid methyl esterHCID 5868586358%

Reaction Steps

To a solution of 4-amino-2-hydroxy benzoic acid methyl ester (836 mg; 5 mmol) and 4-bromobenzaldehyde (926 mg; 5 mmol) in 1 M HOAc in 1,2-dichloroethane (5 mL) was added at once NaBH(OAc)3 (1.49 g; 7 mmol) and the reaction mixture was stirred at room temperature overnight. Water (25 mL) was added and the inhomogeneous mixture was neutralized using solid NaHCO3. The organic layer was isolated, dried, evaporated to dryness and recrystallised from isopropyl ether/dichloromethane/heptane to yield 970 mg (58%) of a yellow solid. NMR and GC-MS in accordance with structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741352B2
Source datasetuspto-grants-2010_06
ORD IDord-27627b1c3a684507b64c67ddba27ff91
Source noteuspto-grants-2010_06