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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846832Generated: October 25, 2026

Methanol → 3-(Phenylethynyl)aniline

https://huagongshe.com/reaction/846832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium sulfide nonahydrateHCID 73972—
ReactantStk331085HCID 800027—
SolventWaterHCID 962—
Product3-(Phenylethynyl)anilineHCID 1343177371%

Reaction Steps

To a 5-liter multi-necked flask fitted with a mechanical stirrer, reflux condenser, and thermometer was charged 215.6 g (0.96 mol) of 3-phenylethynylnitrobenzene obtained as described above, 600.2 g (2.5 mol) of sodium sulfide nonahydrate, 2 liters of methanol, and 500 ml of distilled water. The system is brought to 70° C. for 3 hours at which point the reduction is complete by thin layer chromatography. The reaction mixture is cooled to room temperature and the methanol removed by a rotary evaporator. The concentrate is added to a separatory funnel along with 1 liter of toluene. The toluene layer is separated and washed with distilled water until neutral to pH paper. Concentration of the toluene solution followed by vacuum distillation gave 131 g (0.68 mol, 71% yield) of 3-phenylethynylaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05138028
Source datasetuspto-grants-1992_08
ORD IDord-c9fb7441fe7745b88bb84344fcc952e1
Source noteuspto-grants-1992_08