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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420360Generated: October 25, 2026

Sodium Sulfide → 3-Methoxy-5-nitroaniline

https://huagongshe.com/reaction/420360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfideHCID 14804—
ReactantBenzene, 1-methoxy-3,5-dinitro-HCID 79231—
ReactantSodium BicarbonateHCID 516892—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-Methoxy-5-nitroanilineHCID 275959893.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium bicarbonate (5.62 g, 66.87 mmol) was added to a solution of sodium sulfide (5.5 g, 70.58 mmol) in deionized water (60 mL). When the sodium bicarbonate was completely dissolved, methanol (50 mL) was added, and the solution was cooled to 0° C. A precipitate formed, which was removed by filtration through a Celite pad. The filtered solution was added quickly to a solution of 3,5-dinitroanisole (7.36 g, 37.15 mmol) in methanol (50 mL). The resulting suspension was heated to reflux for 30 min and then the solution was concentrated in vacuo to remove methanol. The aqueous residue was poured into 200 mL of ice-water, and the resulting orange precipitate was collected by filtration. After air-drying, 3-methoxy-5-nitro-phenylamine (5.82 g, 93%) was obtained as light brown solid: ES(+)-HRMS m/e calculated for C7H8N2O3 (M+H)+ 169.0608, found 169.0608.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093385B2
Source datasetuspto-grants-2012_01
ORD IDord-355cf9e651c1456586160eaca41743e6
Source noteuspto-grants-2012_01