HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486802Generated: October 28, 2026
Dimethylformamide → N-Methyl-N-(2-(3-chloro-1-methoxyphenyl)ethyl)-1,4-diaminobutane
https://huagongshe.com/reaction/486802
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(4-Bromobutyl)phthalimide | HCID 93575 | — |
| Reactant | 2-(3-Chloro-4-methoxyphenyl)ethan-1-amine | HCID 2757644 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Methyl-N-(2-(3-chloro-1-methoxyphenyl)ethyl)-1,4-diaminobutane | HCID 67822287 | 47% |
Reaction Steps
A mixture comprising 5.00 g of N-methyl-(2-(3-chloro-4-methoxyphenyl)ethylamine, 9.49 g of N-(4-bromobutyl)phthalimide, 4.16 g of anhydrous potassium carbonate and 50 ml of N,N-dimethylformamide was stirred at a room temperature for 14 hours, followed by the addition of water. The obtained mixture was extracted with ethyl acetate and the ethyl acetate phase was washed with water and a saturated aqueous solution of common salt, dried over anhydrous magnesium sulfate and concentrated, followed by the addition of 50 ml of ethanol and 1.5 ml of hydrazine monohydrate. The obtained mixture was heated under reflux for 2 hours, cooled by allowing to stand and filtered to remove insoluble matter. The filtrate was distilled to obtain 3.16 g of the title compound as a colorless oil (yield: 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292770 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-ea7447b6929e43bd83d7b0172c2c9739 |
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| Source note | uspto-grants-1994_03 |
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