HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571597Generated: October 25, 2026
Hydrogen Sulfide → 2,6-dimethyl-2,3,5,6-tetrahydro-1H-imidazo[1,2-a]imidazole
https://huagongshe.com/reaction/571597
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | N-(2-aminopropyl)propane-1,2-diamine | HCID 96199 | — |
| Solvent | 1-Methylnaphthalene | HCID 7002 | — |
| Product | 2,6-dimethyl-2,3,5,6-tetrahydro-1H-imidazo[1,2-a]imidazole | HCID 58312391 | — |
Reaction Steps
In a 100 mL flask, 0.4078 g of di-(2-aminopropyl)amine (0.00311 mol) was dissolved in 50 mL of 1-methylnaphthalene. Carbon disulfide (0.18 mL, 0.00298 mol) was added. The reaction was stirred for three hours then heated to 200° C. The reaction was heated for four days until production of hydrogen sulfide stopped. The solvent was then removed by distillation. The product was then dissolved in approximately 5 mL of hexanes and 0.5 mL of a 2.0 M ether solution of hydrogen chloride was added. The yield of the precipitate was 0.278 g (53%). The NMR had a doublet at 1.19 ppm, a multiplet at 3.44 ppm, a multiplet at 3.92 ppm and a multiplet at 4.15 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029189B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-0668a5a0741b4e9b93abf1899e8ce733 |
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| Source note | uspto-grants-2015_05 |
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