3-METHYLAMINO-1-PHENYLACETONE HYDROCHLORIDE
3-METHYLAMINO-1-PHENYLACETONE HYDROCHLORIDE Basic information
- Product Name:
- 3-METHYLAMINO-1-PHENYLACETONE HYDROCHLORIDE
- Synonyms:
-
- 3-METHYLAMINO-1-PHENYLACETONE HYDROCHLORIDE
- 3-(METHYLAMINO)PROPIOPHENONE HCL
- 3-Methylaminopropiophenone
- 3-Methylamino-1-Phenyl-1-Acetone HCl
- 3-Methylaminophenylpropanone hydrochloride
- 1-(Methylamino)-3-phenylacetone hydrochloride
- 3-(Methylamino)-1-phenyl-1-propanone hydrochloride
- 1-(MethylaMino)-3-phenylpropan-2-one hydrochloride
- CAS:
- 2538-50-3
- MF:
- C10H14ClNO
- MW:
- 199.68
- Mol File:
- 2538-50-3.mol
3-METHYLAMINO-1-PHENYLACETONE HYDROCHLORIDE Chemical Properties
- Melting point:
- 139-141 °C(Solv: acetone (67-64-1))
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- color
- White to Off-White
- CAS DataBase Reference
- 2538-50-3(CAS DataBase Reference)
3-METHYLAMINO-1-PHENYLACETONE HYDROCHLORIDE Usage And Synthesis
Uses
3-(Methylamino)-1-phenylpropan-1-one Hydrochloride can be used for nontoxic non-irritating wood preservative for toys or teaching appliances.
Synthesis
50-00-0
593-51-1
98-86-2
2538-50-3
Acetophenone (25 mmol), methylamine hydrochloride (27.5 mmol), formaldehyde (35 mmol) and concentrated hydrochloric acid (0.125 mmol) were mixed in ethanol (12.5 mL). The mixture was placed in a sealed container and heated for 20 hours for the reaction. After completion of the reaction, it was cooled to room temperature. The solvent was removed by distillation under reduced pressure, followed by addition of ethyl acetate (25 mL) and continued stirring for 4 hours. The crude product was collected by filtration, washed with ethyl acetate and finally purified by recrystallization from isopropanol to afford the target product 3-(methylamino)-1-phenylpropan-1-one hydrochloride (Product 2a). Yield: 60-70%.
References
[1] Patent: CN103992236, 2016, B. Location in patent: Paragraph 0051-0053
[2] Patent: KR2015/116956, 2015, A. Location in patent: Paragraph 0117-0120
[3] Angewandte Chemie - International Edition, 2005, vol. 44, # 11, p. 1687 - 1689
[4] Angewandte Chemie - International Edition, 2015, vol. 54, # 7, p. 2260 - 2264
[5] Angew. Chem.,
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