Basic information Safety Supplier Related

3-(3-METHOXYPHENYL)-1-PROPENE

Basic information Safety Supplier Related

3-(3-METHOXYPHENYL)-1-PROPENE Basic information

Product Name:
3-(3-METHOXYPHENYL)-1-PROPENE
Synonyms:
  • 3-(3-METHOXYPHENYL)-1-PROPENE
  • 1-methoxy-3-prop-2-enylbenzene
  • Benzene, 1-methoxy-3-(2-propen-1-yl)-
  • 1-Methoxy-3-(2-propen-1-yl)benzene
  • 3-(3-Methoxyphenyl)-1-propene,98% (stabilized with MEHQ)
CAS:
24743-14-4
MF:
C10H12O
MW:
148.2
Mol File:
24743-14-4.mol
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3-(3-METHOXYPHENYL)-1-PROPENE Chemical Properties

Melting point:
124-126 °C
Boiling point:
57°C/0.1mm
Density 
0.978 g/cm3
storage temp. 
2-8°C
form 
crystalline powder
color 
White
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Safety Information

HS Code 
2909309090
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3-(3-METHOXYPHENYL)-1-PROPENE Usage And Synthesis

Synthesis

2398-37-0

106-95-6

24743-14-4

The general procedure for the synthesis of 3-(3-methoxyphenyl)-1-propene from m-bromoanisole and 3-bromo-1-propene was as follows: 1. Preparation of the intermediate 1-methyl-3-methoxybenzene (IIa): 3-bromoanisole (40 g, 0.2138 mol) was dissolved in anhydrous THF (220 mL) and added slowly and dropwise to a solution that had been pre-activated (by addition of a small amount of iodine and briefly heated to initiate the reaction) with magnesium (7.9 g, 0.328 mol) in anhydrous THF (20 mL). After 1 hr of reaction, when the solution was gray and most of the magnesium was dissolved, allyl bromide (28.4 mL, 0.328 mol) was added. The reaction was continued for 3 hours and then quenched with saturated NH4Cl solution. The organic layer was extracted with ether and dried over anhydrous Na2SO4, followed by evaporation of the solvent. The crude product was purified by column chromatography on silica gel (230-400 mesh) using a petroleum ether solution of 3-4% ethyl acetate as eluent to afford the allyl compound as a yellow viscous liquid (24 g, 76% yield).

References

[1] Journal of Organic Chemistry, 2013, vol. 78, # 19, p. 9772 - 9780
[2] Journal of Medicinal Chemistry, 1991, vol. 34, # 8, p. 2638 - 2643
[3] Patent: WO2008/135488, 2008, A1. Location in patent: Page/Page column 43
[4] Tetrahedron, 2010, vol. 66, # 34, p. 6965 - 6976
[5] Chemical and Pharmaceutical Bulletin, 2018, vol. 66, # 7, p. 741 - 747

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