HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834495Generated: October 30, 2026
Epichlorohydrin → 1-Amino-3-({[4-(aminomethyl)cyclohexyl]methyl}amino)propan-2-ol
https://huagongshe.com/reaction/1834495
Participants
| Role | Name | HCID | Charge |
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| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1,4-Cyclohexanedimethanamine | HCID 17354 | — |
| Reactant | 1-Chloro-2-propanol | HCID 31370 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Amino-3-({[4-(aminomethyl)cyclohexyl]methyl}amino)propan-2-ol | HCID 20373430 | — |
Reaction Steps
1,4-Cyclohexanebis(methylamine) (14.2 g., 0.1 mole) is dissolved in 50 ml. of anhydrous methyl alcohol and the solution cooled to +5° C. in an ice bath. Epichlorohydrin (9.3 g., 0.1 mole) is added in a 2-minute period and the temperature maintained at +5° C. for 2 hours; reaction is allowed to continue at 10° C-15° C. until thin layer chromatography of an aliquot (silica gel plate with development using a solution of 1 volume concentrated aqueous ammonium hydroxide in 4 volumes of methyl alcohol) indicated nearly complete conversion of the starting diamine to the propylene chlorohydrin. The solution is then added to 100 ml. of dry with methyl alcohol previously saturated at 0° C. with dry ammonia gas by continuous dropwise flow at +5° C. with good agitation and external cooling. After stirring 2 hours at °5° C., it is allowed to warm to 20° C. and mixed overnight. The reaction is competed by heating at 45° C.-55° C. for 6 hours. The solvent and ammonia was removed by stripping and the product purified using fractional distillation under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04070400 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-2323f2d7a0ab4edcb487269133029d6f |
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| Source note | uspto-grants-1978_01 |
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