HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060203Generated: October 25, 2026
Isophorone diamine → HCID 18667850, compound
https://huagongshe.com/reaction/1060203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isophorone diamine | HCID 17857 | — |
| Reactant | 2,2,6-Trimethyl-4H-1,3-dioxin-4-one | HCID 79368 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 18667850 | HCID 18667850 | 98% |
Reaction Steps
To isophoronediamine (139.24 g, 0.819 mol) in xylene (525 ml) at 120° C. was added with stirring 2,2,6-trimethyl-1,3-dioxen-4-one (232.51 g, 1.637 mol) in xylene (525 ml) over 10 minutes, during which the temperature decreased to 103° C. Vigorous effervescence and distillation of acetone (through a Vigreux column) immediately commenced. Pot temperature was increased to 120° C. over 15 minutes, and to 139° C. over a further 30 minutes, with collection of acetone distillate. After cooling to 58° C., supernatant solution was separated from deposited gum, which was dissolved in dichloromethane. Removal of solvent from combined solutions and drying (91° C./100 Pa) gave 1-acetoacetamido-3-acetoacetamidomethyl-3,5,5-trimethylcyclohexane (270.21 g, 98%), (AAMTCH), which was crushed to a light yellow powder, mp 144-147° C. (mixture of E and Z isomers), and identified by 1H-NMR, 13C-NMR, FT-IR and Raman spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06521716B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-1495e1282f644d5ebefce3b5ac4853f1 |
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| Source note | uspto-grants-2003_02 |
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