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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771864Generated: November 1, 2026

Water → Methyl 4-(4-aminophenylthio)-3-nitrobenzoate

https://huagongshe.com/reaction/1771864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-AminothiophenolHCID 14510—
ReactantMethyl 4-chloro-3-nitrobenzoateHCID 735797—
SolventDimethylformamideHCID 6228—
SolventDiisopropyl EtherHCID 7914—
ProductMethyl 4-(4-aminophenylthio)-3-nitrobenzoateHCID 5937680490%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-chloro-3-nitrobenzoic acid methyl ester (15.0 g, 68 mmol), 4-aminothiophenol (8.8 g, 68 mmol) and K2CO3 (11.8 g, 85 mmol) in DMF (150 mL) was heated at 90° C. for 1.5 hours, cooled to room temperature, and then poured into H2O (450 mL) under stirring. The aqueous mixture was extracted with ethyl acetate (400 mL). The extract was washed with H2O (3 times) and brine, dried over MgSO4, and evaporated to give the crude produce as orange crystal. The crude product was suspended in 150 mL of i-Pr2O and stirred at room temperature for 1 hour. The crystal was collected by filtration, washed with i-Pr2O and dried at 60° C. for 3 days under reduced pressure gave purified title compound as orange crystal (18.6 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249138B2
Source datasetuspto-grants-2016_02
ORD IDord-0d736717c6b949b4abecc32bd1afd42c
Source noteuspto-grants-2016_02