2-Bromo-1-(4-dimethylamino-phenyl)-ethanone

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2-Bromo-1-(4-dimethylamino-phenyl)-ethanone Basic information
Product Name:2-Bromo-1-(4-dimethylamino-phenyl)-ethanone
Synonyms:BUTTPARK 82\50-86;2-BROMO-4'-DIMETHYLAMINOACETOPHENONE;4-(Dimethylamino)phenacyl bromide;4-(Dimethylamino)phenacyl bromide 97%;2-BroMo-1-[4-(diMethylaMino)phenyl]ethan-1-one;4-(Dimethylamino)phenacylbromide97%;2-Bromo-4'-(dimethylamino)acetophenone, 2-Bromo-1-[4-(dimethylamino)phenyl]ethan-1-one;Ethanone, 2-bromo-1-[4-(dimethylamino)phenyl]-
CAS:37904-72-6
MF:C10H12BrNO
MW:242.11
EINECS:
Product Categories:blocks;Bromides
Mol File:37904-72-6.mol
2-Bromo-1-(4-dimethylamino-phenyl)-ethanone Structure
2-Bromo-1-(4-dimethylamino-phenyl)-ethanone Chemical Properties
Melting point 89-92
Boiling point 330.2±22.0 °C(Predicted)
density 1.406±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. Inert atmosphere,2-8°C
solubility Chloroform (Sparingly), DMSO (Slightly, Sonicated)
form Solid
pka1.56±0.12(Predicted)
color Yellow to Dark Yellow
InChI1S/C10H12BrNO/c1-12(2)9-5-3-8(4-6-9)10(13)7-11/h3-6H,7H2,1-2H3
InChIKeyYWNKTZFJKMGVRP-UHFFFAOYSA-N
SMILESCN(C)c1ccc(cc1)C(=O)CBr
Safety Information
Hazard Codes Xi
WGK Germany WGK 3
Hazard Note Harmful/Irritant/Keep Cold
HS Code 2934309090
Storage Class11 - Combustible Solids
MSDS Information
2-Bromo-1-(4-dimethylamino-phenyl)-ethanone Usage And Synthesis
Uses2-Bromo-1-(4-dimethylaminophenyl)ethanone can be used as potential biomarkers for respiratory illness.
Synthesis
Ethanone, 2,2-dibromo-1-[4-(dimethylamino)phenyl]-

210832-81-8

2-BROMO-1-(4-DIMETHYLAMINO-PHENYL)-ETHANONE

37904-72-6

The general procedure for the synthesis of 2-bromo-1-(4-(dimethylamino)phenyl)ethanone from the compound (CAS: 210832-81-8) was as follows: 5.1 g (1 eq.) of the raw material was dissolved in 30 mL of THF, and cooled to 0°C. Subsequently, a mixed solution consisting of diethyl phosphite (2.04 mL, 1 eq.) and triethylamine (2.4 mL, 1.1 eq.) in 12 mL of THF was added slowly and dropwise. The reaction mixture was stirred at room temperature for 6 hours. Upon completion of the reaction, the solvent was removed by rotary evaporation and the residue was poured into 200 mL of ice water. The resulting precipitate was collected by filtration, washed with water and dried under vacuum to give the green solid product 3 in 89% yield. The structure of the product was confirmed by nuclear magnetic resonance hydrogen (1H NMR, CDCl3) and carbon (13C NMR, CDCl3) spectra: 1H NMR (CDCl3) δ 2.97 (s, 6H, 2×CH3), 4.45 (s, 2H, CH2), 6.57 (d, 2H, J = 9.0 Hz, 2×CHAr), 7.72 (d, 2H, CHAr); 13C NMR (CDCl3) δ 31.3 (1C, CH2), 40.4 (2C, CH3), 111.1 (2C, CHAr), 121.8 (1C, Cq), 131.6 (2C, CHAr), 154.1 (1C, Cq), 189.7 (1C, Cq).

References[1] Tetrahedron Letters, 1998, vol. 39, # 28, p. 4987 - 4990
[2] Patent: US2007/258887, 2007, A1. Location in patent: Page/Page column 28; 39-40
[3] Chemical Communications, 2016, vol. 52, # 90, p. 13277 - 13280
[4] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 10, p. 2966 - 2968
[5] ACS Medicinal Chemistry Letters, 2013, vol. 4, # 7, p. 596 - 600
2-Bromo-1-(4-dimethylamino-phenyl)-ethanone Preparation Products And Raw materials
Raw materialsEthanone, 2,2-dibromo-1-[4-(dimethylamino)phenyl]--->Triethylamine-->Diethyl phosphite-->Tetrahydrofuran
Tag:2-Bromo-1-(4-dimethylamino-phenyl)-ethanone(37904-72-6) Related Product Information
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