Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,1'-[1,4-Phenylenedi(ethene-2,1-diyl)]bis(4-nitrobenzene) | HCID 54469894 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53710909 | HCID 53710909 | 96.2% |
Reaction Steps
25.9 g of 1,4-bis(4-nitrostyryl)benzene were added to a mixture consisting of 50 g of iron powder, 12 ml of undiluted hydrochloric acid, 50 ml of water and 800 ml of N,N-dimethyl formamide and subjected to 1.5 hours' intense stirring at a temperature in the range of from 90° to 100° C. Thereafter, the pH value was adjusted to be 8 by means of 10% aqueous solution of sodium carbonate while thus heating, and the undissolved matter was filtered. From the resulting filtrate were separated yellow crystals, and these crystals were collected by filtering, washed in water, dried, and thereafter recrystallized from N,N-dimethyl formaldehyde, whereby there were obtained 20.9 g (yield rate: 95.7%) of 1,4-bis(4-aminostyryl)benzene in the form of yellow crystals (melting point: 300° C. or more).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04242260 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-bd4a35b4a81046acbf8b0f820768eb7c |
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| Source note | uspto-grants-1980_12 |
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