3'-methoxypropiophenone CAS 37951-49-8

Introduction:Basic information about 3'-methoxypropiophenone CAS 37951-49-8, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

3'-methoxypropiophenone Basic information

Product Name:3'-methoxypropiophenone
Synonyms:1-(3-methoxy-phenyl)propan-1-one;1-(3-Methoxyphenyl)-1-propanone;1-Propanone, 1-(3-methoxyphenyl)-;3'-Methoxypropiophenone;3-methoxypropiophenone;3'-Methoxypropiophenone, 99%
CAS:37951-49-8
MF:C10H12O2
MW:164.2
EINECS:253-729-3
Product Categories:
Mol File:37951-49-8.mol

3'-methoxypropiophenone Chemical Properties

Boiling point 259℃
density 1.0812
refractive index 1.5230 (estimate)
storage temp. Sealed in dry,Room Temperature
AppearanceColorless to light yellow Liquid
InChIInChI=1S/C10H12O2/c1-3-10(11)8-5-4-6-9(7-8)12-2/h4-7H,3H2,1-2H3
InChIKeyLPDJHUUWTGXTCU-UHFFFAOYSA-N
SMILESC(C1=CC=CC(OC)=C1)(=O)CC

Safety Information

HS Code 2914500090

3'-methoxypropiophenone Usage And Synthesis

Chemical Properties3'-methoxypropiophenone is an organic compound belonging to the ketone class of compounds. It is a yellow to yellow brown liquid with a boiling point of 259 °C. 
Uses3'-methoxypropiophenone has a wide range of applications in the fields of medicine, chemistry, and industry.
PreparationPreparation by reaction of ethylmagnesium bromide,
with m-methoxybenzonitrile (m.p. 60°)
with 3-methoxybenzaldehyde and oxidation of the resulting 1-(3-methoxyphenyl)-1-propanol with sodium dichromate in sulfuric acid (70%).
Synthesis

925-90-6

152121-82-9

37951-49-8

Under argon protection, 3,N-dimethoxy-N-methylbenzamide (5.86 g, 30.0 mmol) was dissolved in THF (150 mL) and cooled to 0°C. Slowly add ethylmagnesium bromide (0.960 mol/L THF solution, 100 mL, 96.0 mmol). After addition, bring to room temperature and stir for 3.5 hours. Upon completion of the reaction, the reaction was quenched with 1 mol/L hydrochloric acid and subsequently extracted with ethyl acetate. The organic layers were combined, washed sequentially with water and saturated saline, and dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded m-methoxypropiophenone (4.93 g, 30.0 mmol, quantitative yield) as a yellow oil.1H-NMR (400 MHz, CDCl3): δ 1.23 (3H, t, J = 7.3 Hz), 3.00 (2H, q, J = 7.3 Hz), 3.86 (3H, s), 7.10 (1H, dd, J = 7.9 , 2.4 Hz), 7.37 (1H, t, J = 7.9 Hz), 7.50 (1H, t, J = 2.4 Hz), 7.54 (1H, d, J = 7.9 Hz).

References[1] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 1, p. 375 - 381
[2] Patent: WO2007/62190, 2007, A2. Location in patent: Page/Page column 29; 30
[3] Patent: WO2007/62145, 2007, A2. Location in patent: Page/Page column 41
[4] Patent: WO2007/44796, 2007, A2. Location in patent: Page/Page column 35-36
[5] Angewandte Chemie - International Edition, 2016, vol. 55, # 52, p. 16115 - 16118

3'-methoxypropiophenone Preparation Products And Raw materials

Raw materials3'-Hydroxypropiophenone-->3,N-DIMETHOXY-N-METHYLBENZAMIDE-->3-Methoxybenzonitrile-->Benzenemethanol, α-?ethenyl-?3-?methoxy--->3-Bromoanisole-->Propionitrile-->Ethylmagnesium bromide-->Iodomethane-->Tetrahydrofuran-->Hydrochloric acid
Preparation Products1-(3-Methoxyphenyl)-2-Methylpropan-1-ol-->(S)-3-(dimethylamino)-1-(3-methoxyphenyl)-2-methylpropan-1-one
3-Methoxyfuran-2-carbaldehyde CAS 32487-58-4
3-Methoxythiophene CAS 17573-92-1
Recommended......
TOP