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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071878Generated: October 31, 2026

Ammonia → 1-Amino-3-({[4-(aminomethyl)cyclohexyl]methyl}amino)propan-2-ol

https://huagongshe.com/reaction/2071878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEpichlorohydrinHCID 7835—
ReactantAmmonium HydroxideHCID 14923—
Reactant1,4-CyclohexanedimethanamineHCID 17354—
Reactant1-Chloro-2-propanolHCID 31370—
SolventMethanolHCID 887—
Product1-Amino-3-({[4-(aminomethyl)cyclohexyl]methyl}amino)propan-2-olHCID 20373430—

Reaction Conditions

Temperature20 °C

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°-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 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°-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049417
Source datasetuspto-grants-1977_09
ORD IDord-c6ea3f60e7444979a4763b1e39a658b2
Source noteuspto-grants-1977_09