HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390Generated: October 29, 2026
Potassium Hydroxide → HCID 15308372, compound
https://huagongshe.com/reaction/2390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N,N'-bis-(imidazolin-2-yl)ethylenediamine hydrobromide | HCID 19690351 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15308372 | HCID 15308372 | — |
Reaction Steps
In 1,400 ml of methanol, 200 g of N,N'-bis-(imidazolin-2-yl)ethylenediamine hydrobromide was dissolved and to the solution, 63 g of 85% potassium hydroxide was then added and stirred for 1 hr at 25° C. After potassium bromide precipitated was filtered out, methanol was removed by distillation to obtain N,N'-bis(imidazolin-2-yl)ethylenediamine as a solid. In 680 ml of ethanol, 34 g (0.1 mol) of 4-(phenylsulfonyl)phenylsulfonylacetic acid was heated to dissolve. To the cooled solution was then added 9.8 g (0.05 mol) of N,N'-bis(imidazolin-2-yl)ethylenediamine in ethanol and the resulting mixture was cooled to 10° C. A crystal precipitated was filtered off, washed and air-dried to obtain 42 g of the intended Compound 3 as crystals. NMR (heavy methanol): δ8.2 (q, 8H), 8.0 (m, 4H), 7.6 (m, 6H), 3.7 (s, 8H), 3.4 (s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05728879 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-e88dc59bf100482c82d3a74374503023 |
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| Source note | uspto-grants-1998_03 |
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