HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374361Generated: October 30, 2026
Ammonia → 2-Methyl-2-propylpentane-1,5-diamine
https://huagongshe.com/reaction/374361
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | 4-Formyl-4-methylheptanenitrile | HCID 14993119 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | 2-Methyl-2-propylpentane-1,5-diamine | HCID 14993120 | — |
| Product | 3-Methyl-3-propylpiperidine | HCID 14993121 | — |
Reaction Steps
Example 1 was repeated using 2-methyl-2-propyl-4-cyanobutanal as the starting material. 33.5 g per hour of 2-methyl-2-propyl-4-cyanobutanal (purity 88.9%, 29.8 g, 0.195 mol) and 1400 ml (840 g, 49.4 mol) per hour of liquid ammonia were pumped at 250 bar and 60° C. through the imination reactor. The product stream was subsequently passed through the hydrogenation reactor from bottom to top at 250 bar and 120° C. while simultaneously passing 100 l(S.T.P.)/h (4.5 mol) of hydrogen through the reactor. The product stream was decompressed to atmospheric pressure and NH3 was removed by distillation. The product from 37.5 hours was separated 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 mmHg) and 842.1 g of 2-methyl-2-propylpentane-1,5-diamine (b.p.=78°- 81° C./2 mmHg). The diamine yield was 72.9% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05166443 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-0ee0872b2df7417bac59ccde2acdd8a6 |
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| Source note | uspto-grants-1992_11 |
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