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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462648Generated: October 26, 2026

Calcium Carbonate → n-Methyl-p-aminophenol

https://huagongshe.com/reaction/462648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCalcium CarbonateHCID 10112—
Reactantp-(N-methylamino)phenol sulfateHCID 10198132—
SolventWaterHCID 962—
Productn-Methyl-p-aminophenolHCID 593175%

Reaction Steps

A mixture of p-(N-methylamino)phenol sulfate (13.6 g, 80 mmol), calcium carbonate (15 g, 160 mmol and water (30 mL) was triturated with mortar and pestil, and repeatedly extracted with ether (8×60 mL). The combined ether extracts were washed with water, and dried with anhydrous sodium sulfate. The solution was then evaporated to dryness, and the solid residue dried in vacuum over phosphorus pentoxide at ambient temperature to provide 7.32 g (60 mmol) of p-(N-methylamino)phenol. To anhydrous ether (240 mL) was added pyridine (4.8 mL, 60 mmol) and p-(N-methylamino)phenol 7.32 g (60 mmol). The resulting solution was added dropwise to a cooled solution (0° C.) of phosphorous oxychloride (5.4 mL, 60 mmol) in ether (100 mL) with stirring under nitrogen. The reaction mixture was stirred at room temperature for 60 minutes, filtered, and the filtrate added dropwise to a saturated solution of anhydrous ammonia in ether (450 mL, 0° C.). The reaction mixture was allowed to warm to room temperature with stirring (60 minutes). A white precipitate formed which was isolated by filtration, rinsed with ether and dried in vacuum over phosphorous pentoxide at room temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04517004
Source datasetuspto-grants-1985_05
ORD IDord-7935959c2cec442194fd71f751569012
Source noteuspto-grants-1985_05