HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071877Generated: October 26, 2026
Ethylene Oxide → 2-({[4-(Aminomethyl)cyclohexyl]methyl}amino)ethan-1-ol
https://huagongshe.com/reaction/2071877
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | 1,4-Cyclohexanedimethanamine | HCID 17354 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-({[4-(Aminomethyl)cyclohexyl]methyl}amino)ethan-1-ol | HCID 20373428 | — |
Reaction Steps
A solution of 14.2 gm. (0.1 mole) of 1,4-cyclohexanebis(methylamine) in 150 ml. anhydrous methyl alcohol and under an atmosphere of nitrogen is warmed to 45°-50° C. In a 20 minute period, there is introduced with good agitation and beneath the liquid surface a total of 1.1 gm. (0.025 mole) of ethylene oxide in gaseous form. The reaction temperature is maintained at 45°-50° C. for an additional one-half hour after stopping the addition of ethylene oxide. The methyl alcohol is removed by distillation at atmospheric pressure; excess 1,4-cyclohexanebis(methylamine) is readily separated from the product by fractionation under reduced pressure. Only monoethoxylated compound remained and could be used as such or further purified by distillation at reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04049417 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-ec8dd98f7c194c04b84ca90ee87f565a |
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| Source note | uspto-grants-1977_09 |
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