HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986340Generated: October 30, 2026
Acetone → 1,3,3,4-Tetramethylpiperazin-2-one
https://huagongshe.com/reaction/986340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,3,3,4-Tetramethylpiperazin-2-one | HCID 18003351 | — |
Reaction Steps
8.8 g N,N'-dimethyl-ethylene diamine, 12.0 g CHCl3, and 6.0 g acetone are placed in a 250 ml flask in an ice-bath, and 1.1 g BTAC added. To provide a homogeneous organic liquid phase, 100 ml dichloromethane is added. Then 40 ml conc NaOH (50% by wt) is dripped into the flask over about 30 mins. The reaction is allowed to proceed for about 5 hr and the reaction product is worked up by dissolving in a minimum amount of water, and then enough dichloromethane is added to provide two distinct layers. The aqueous layer is extracted twice with 50 ml dichloromethane, washed and worked up is a conventional manner. Upon distillation the product is obtained. The foregoing structure of the compound is supported by IR, NMR, GC and mass spectrometer data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04711957 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-e1a2a07c2e984f1b918b1b1ca1990dbc |
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| Source note | uspto-grants-1987_12 |
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