4-METHOXY-BETA-NITROSTYRENE

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CAS:5576-97-6
4-METHOXY-BETA-NITROSTYRENE Basic information
Product Name:4-METHOXY-BETA-NITROSTYRENE
Synonyms:4-Methoxy-nitrostyrene;trans-4-methoxy-beta-nitrosytrene;4-METHOXY-B-NITROSTYRENE;trans-4-methoxy-β-nitrostyrene;(E)-1-(4-Methoxyphenyl)-2-nitroethene;(E)-1-Nitro-2-(4-methoxyphenyl)ethene;1-[(E)-2-Nitrovinyl]-4-methoxybenzene;4-[(E)-2-Nitroethenyl]anisole
CAS:5576-97-6
MF:C9H9NO3
MW:179.17
EINECS:
Product Categories:Acyclic;Alkenes;Organic Building Blocks
Mol File:5576-97-6.mol
4-METHOXY-BETA-NITROSTYRENE Structure
4-METHOXY-BETA-NITROSTYRENE Chemical Properties
Melting point 86-88 °C(lit.)
Boiling point 317.0±17.0 °C(Predicted)
density 1.189±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility chloroform: soluble25mg/mL, clear, yellow
AppearanceLight yellow to yellow Solid
BRN 2047935
CAS DataBase Reference5576-97-6
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 2909309090
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
4-METHOXY-BETA-NITROSTYRENE Usage And Synthesis
Chemical PropertiesYellow needle-like (ethanol) or flake-like (benzene) crystals. Melting point 86-88°C.
Usestrans-4-Methoxy-β-nitrostyrene acts as guest molecule and forms guest molecules forming co-crystal phases with the d-form of robust syndiotactic polystyrene (sPS). It may be employed as a Michael acceptor in the synthesis of proline based chiral ionic liquid catalysts with two five-membered unsaturated aza-heterocycles.
DefinitionChEBI: 1-(4-Methoxyphenyl)-2-nitroethylene is a member of methoxybenzenes.
General Descriptiontrans-4-Methoxy-β-nitrostyrene participates in the Michael reaction on carbapenam intermediate.
Synthesis
4-Methoxystyrene

637-69-4

1-(4-Methoxyphenyl)-2-nitroethylene

3179-10-0

GENERAL STEPS: To a 25 mL sealed tube was added 4-methoxystyrene (0.5 mmol), sodium nitrite (1.5 eq.), potassium persulfate (2.0 eq.), TEMPO (1.2 eq.) and 1,2-dichloroethane (2 mL). The reaction mixture was stirred at 100 °C for 24 hours. After the reaction was completed, it was cooled to room temperature. Extraction was performed by adding dichloromethane (2 mL) and water (5 mL). The organic layer was separated and the aqueous phase was further extracted with dichloromethane (5 mL x 3). The organic layers were combined, dried over anhydrous sodium sulfate and filtered. After the solvent was removed by concentration under reduced pressure, the residue was purified by column chromatography using petroleum ether/ethyl acetate as eluent to give pure 1-methoxy-4-(2-nitrovinyl)benzene.

References[1] Tetrahedron Letters, 2016, vol. 57, # 1, p. 80 - 84
[2] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1993, # 12, p. 2399 - 2404
[3] Synlett, 2014, vol. 25, # 14, p. 1997 - 2000
[4] Journal of the American Chemical Society, 2013, vol. 135, # 9, p. 3355 - 3358
[5] Journal of Organic Chemistry, 2013, vol. 78, # 12, p. 5949 - 5954
Tag:4-METHOXY-BETA-NITROSTYRENE(5576-97-6) Related Product Information
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