Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium sulfide nonahydrate | HCID 73972 | — |
| Reactant | Stk331085 | HCID 800027 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(Phenylethynyl)aniline | HCID 13431773 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05138028 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-c9fb7441fe7745b88bb84344fcc952e1 |
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| Source note | uspto-grants-1992_08 |
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