HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074306Generated: October 26, 2026
1,4-Benzenedimethanamine → 1,4-Dicyanobenzene
https://huagongshe.com/reaction/1074306
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Benzenedimethanamine | HCID 68315 | — |
| Reactant | [1-(Aminomethyl)cyclohexyl]methanamine | HCID 71994 | — |
| Product | 1,4-Dicyanobenzene | HCID 12172 | — |
Reaction Steps
5.1 g of terephthalonitrile, 1.0 g of catalyst (Ni 5136P from Harshaw/Filtrol--contains 65% nickel on a silica-alumina support), and about 85 g of ethanol/ammonia (contains about 10 wt % ammonia) were charged to a 300 cc stainless steel pressure reactor. After a nitrogen purge, the vessel was charged to a pressure of 500 to 1000 psi with hydrogen. The temperature was then increased until the reaction temperature of 150° C. had been obtained (typically 20-30 min). After the desired reaction interval, the contents were cooled and sampled. Product analysis and conversion were determined by gas chromatography. Yields of para-xylylenediamine varied between 63-81% depending on hydrogen pressure and reaction time which is preferrably from 2 to 8 hours. The remainder of the product was saturated para-xylylenediamine (1.4 bis (aminomethyl) cyclohexane. Table IV sets forth specific examples of reactions run to obtain the diamines from hydrogenation of terephthalonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04973746 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-6b095c98046f4a018ffc8999ecc5e1bc |
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| Source note | uspto-grants-1990_11 |
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