HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65832Generated: October 29, 2026
Salicylaldehyde → N,N'-bis-(2-hydroxybenzyl)-2,5-diamino-2,5-dimethyl-hexane
https://huagongshe.com/reaction/65832
Participants
| Role | Name | HCID | Charge |
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| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | 2,5-Hexanediamine, 2,5-dimethyl- | HCID 90189 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N,N'-bis-(2-hydroxybenzyl)-2,5-diamino-2,5-dimethyl-hexane | HCID 22756075 | 34% |
Reaction Steps
55.0 g of a bisazomethine prepared from 2 mols of salicylaldehyde and 1 mol of 2,5-diamino-2,5-dimethylhexane and with a melting point of 111°-112° C. are hydrogenated for 2 hours in 250 ml of ethanol in an autoclave in the presence of 5.5 g of Raney nickel at 100° C. and under a pressure of 80 atmospheres. The catalyst is filtered off and the filtrate is concentrated. The residue is recrystallised from 220 ml of ispropanol, collected by filtration, washed with n-hexane and dried in vacuo, affording 18.9 g (34% of theory) of N,N'-bis-(2-hydroxybenzyl)-2,5-diamino-2,5-dimethyl-hexane with a melting point of 102°-106° C. Two recrystallisations from a mixture of cyclohexane and ethanol yield 15.2 g of pure product with a melting point of 124°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04129556 |
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| Source dataset | uspto-grants-1978_12 |
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| ORD ID | ord-0460bd2a44ee4b5daf634964946d1530 |
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| Source note | uspto-grants-1978_12 |
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