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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883958Generated: November 4, 2026

Acetic Acid → 4-(4-Benzylamino-2-nitro-phenylsulfanyl)-phenol

https://huagongshe.com/reaction/883958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-(4-Amino-2-nitro-phenylsulfanyl)-phenolHCID 66808437—
SolventMethanolHCID 887—
Product4-(4-Benzylamino-2-nitro-phenylsulfanyl)-phenolHCID 6680847677.7%

Reaction Steps

A solution of the product of Example 62A (0.63 g, 2.4 mmol), benzaldehyde (0.24 g, 2.3 mmol) and sodium cyanoborohydride (0.15 g, 2.4 mmol) in methanol (10 mL) containing 1% acetic acid was stirred at room temperature for 16 hours. The reaction mixture was quenched with water (20 mL) and the resultant solution was concentrated under vacuum to a yellow solid. The solid was dissolved in ethyl acetate (50 mL), and washed with water, 10% sodium bicarbonate and 10% sodium chloride. The organic layer was dried over anhydrous sodium sulfate, filtered and solvent removed under vacuum leaving a light yellow oil. The oil was purified by silica gel chromatography eluting with 1% methanol in methylene chloride to provide the title compound (0.63 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236950B2
Source datasetuspto-grants-2012_08
ORD IDord-f30a750b3b4f4d21aba242ae4ade1b8b
Source noteuspto-grants-2012_08