HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441119Generated: November 2, 2026
1,3-Benzenedimethanamine → HCID 67061088, compound
https://huagongshe.com/reaction/1441119
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Benzenedimethanamine | HCID 15133 | — |
| Reactant | HCID 54300175 | HCID 54300175 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 67061088 | HCID 67061088 | 99% |
Reaction Steps
To a 1000 ml flask replaced with nitrogen 257.4 g (1.26 mol) of allyl-bicyclo 2.2.1!hept-5-ene-2,3-dicarboxylic acid anhydride and 300 ml of xylene were charged. To the mixture was added 81.4 g (0.60 mol) of m-xylylenediamine over 1.5 hours with heating and stirring while refluxing xylene. The reaction was continued for 3 hours while separating and removing water produced by the reaction by a water separator, and then the solvent, xylene, was removed by distillation. Thereafter, the content of the flask was treated with heat at 200° C. under reduced pressure of 1 Torr for 1 hour while stirring, thus obtaining 301.8 g (yield: 99%) of the target N,N'-m-xylylene-bis(allyl-bicyclo 2.2.1!hept-5-ene-2,3-dicarboximide), of which the chemical structure is shown by the following formula 6!. This compound is hereinafter abbreviated to BANI-mX. ##STR10##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05502207 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-ba172605fdf948348feb5151b21f035a |
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| Source note | uspto-grants-1996_03 |
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