ChemicalBook--->CAS DataBase List--->126055-32-1

126055-32-1

126055-32-1 Structure

126055-32-1 Structure
IdentificationBack Directory
[Name]

1-(2-Chloroethyl)-4-Methylpiperazine hydrochloride
[CAS]

126055-32-1
[Synonyms]

-4-methylpiperazine hydrochloride
(2E)-3-(5-methyl-54-furyl)acrylic acid
1-(2-Chloroethyl)-4-methylpiperazine HCl
1-(2-Chloroethyl)-4-Methylpiperazine hydrochloride
Piperazine, 1-(2-chloroethyl)-4-methyl-, hydrochloride (1:1)
[Molecular Formula]

C7H16Cl2N2
[MDL Number]

MFCD12031872
[MOL File]

126055-32-1.mol
[Molecular Weight]

199.121
Chemical PropertiesBack Directory
[Melting point ]

279-280 °C (decomp)
[storage temp. ]

Inert atmosphere,Room Temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

1-(2-Chloroethyl)-4-Methylpiperazine hydrochloride(126055-32-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Methylpiperazine

109-01-3

1-Bromo-2-chloroethane

107-04-0

1-(2-CHLORO-ETHYL)-4-METHYL-PIPERAZINE

5753-26-4

1. 10 mL of 25% NaOH solution and 1 mL (9 mmol) of N-methylpiperazine were added sequentially to the reaction flask. 2. the mixture was heated to 50 °C and 1.8 mL (18 mmol) of 1-bromo-2-chloroethane was added slowly and dropwise. 3. The reaction mixture was kept at 50 °C with stirring for 6 hours and subsequently cooled to room temperature. 4. The reaction solution was extracted using ethyl acetate, the extract was washed with saturated brine solution, dried over anhydrous sodium sulfate and filtered. 5. The filtrate was concentrated to dryness under reduced pressure and a small amount of ethanol/NaOH solution was added dropwise to the residue. 6. The mixture was shaken and allowed to stand in a refrigerator and subsequently concentrated to dryness under reduced pressure to give 0.43 g of the white solid product 1-(2-chloroethyl)-4-methylpiperazine dihydrochloride in 23% yield. 7. The melting point of the product was determined to be 227-230 °C.

[References]

[1] Patent: US2013/85140, 2013, A1. Location in patent: Paragraph 0064; 0065
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