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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742828Generated: October 30, 2026

Ammonia → 2-Methyl-2-propylpentane-1,5-diamine

https://huagongshe.com/reaction/742828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-Formyl-4-methylheptanenitrileHCID 14993119—
ReactantHCID 178418361HCID 178418361—
Product2-Methyl-2-propylpentane-1,5-diamineHCID 14993120—
Product3-Methyl-3-propylpiperidineHCID 14993121—

Reaction Steps

33.5 g of 2-methyl-2-propyl-4-cyanobutanal (purity: 88.9%, 29.8 g, 0.195 mol) and 1,400 ml (840 g, 49.4 mol) of liquid ammonia were pumped per hour at 250 bar and 60° C. through a tubular reactor (diameter: 16 mm, filling level: 50 cm, oil-heated twin jacket) which was arranged upstream of the hydrogenation reactor and was filled with 63.5 g (100 ml) of TiO2 (anatase) in the form of 1.5 mm pellets. The product was then passed through the hydrogenation reactor from bottom to top at 250 bar and 120° C. while simultaneously passing through 100 l (s.t.p.)/h (4.5 mol) of hydrogen. After decompression to atmospheric pressure, NH3 was removed by distillation. The product from 37.5 hours was separated into its components by fractional distillation on a 30 cm packed column (3 mm glass rings), giving 277.0 g of 3-methyl-3-propylpiperidine (b.p.=46° C./2 mm Hg) and 842.1 g of 2-methyl-2-propylpentane-1,5-diamine (b.p.=78°-81° C./2 mm Hg). The yield of diamine was 72.9% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554787
Source datasetuspto-grants-1996_09
ORD IDord-fc5be8901c7e4a2fa7788e84a3a1cfab
Source noteuspto-grants-1996_09