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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

Reaction equation

Participants

RoleNameHCIDCharge
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

Temperature5 °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° 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04070400
Source datasetuspto-grants-1978_01
ORD IDord-2323f2d7a0ab4edcb487269133029d6f
Source noteuspto-grants-1978_01