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1-tert-butyl-4-ethoxybenzene

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Identification
Molecular formula
C12H18O
CAS number
122-66-7
IUPAC name
1-tert-butyl-4-ethoxy-benzene
State
State
At room temperature, 1-tert-butyl-4-ethoxybenzene is a liquid.
Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
178.27g/mol
Molar mass
178.2730g/mol
Density
0.8720g/cm3
Appearence

1-tert-butyl-4-ethoxybenzene is a colorless liquid. It is primarily noted for its use in organic synthesis and industrial applications. It typically exhibits a clear, watery consistency.

Comment on solubility

Solubility of 1-tert-butyl-4-ethoxy-benzene

1-tert-butyl-4-ethoxy-benzene, a substituted aromatic compound, showcases intriguing solubility characteristics.

When evaluating the solubility of this compound, consider the following points:

  • Polarity: The compound features a non-polar tert-butyl group and a moderately polar ethoxy group, leading to an ambiguous solubility profile.
  • Solvents: It tends to be more soluble in organic solvents such as hexane, benzene, and ethyl acetate due to the non-polar nature of the aromatic ring and the tert-butyl group.
  • Aqueous Solutions: In contrast, its solubility in water is considerably low as the polar ethoxy group is outweighed by the larger non-polar components, resulting in a hydrophobic character.

In summary, while 1-tert-butyl-4-ethoxy-benzene may dissolve well in organic solvents, its solubility in water is quite limited, illustrating the classic principle of "like dissolves like." Understanding the solubility behavior of this compound is essential for applications in organic synthesis and material science.

Interesting facts

Exploring 1-tert-butyl-4-ethoxy-benzene

1-tert-butyl-4-ethoxy-benzene, often simply referred to as a derivative of ethylbenzene, is a fascinating compound within the field of organic chemistry. Here are some intriguing aspects of this compound:

  • Structure and Stability: This compound features a robust structure due to the presence of the tert-butyl group, which imparts remarkable stability to the benzene ring. The bulky tert-butyl group helps to enhance steric hindrance, reducing the likelihood of electrophilic attack.
  • Synthesis Insights: 1-tert-butyl-4-ethoxy-benzene can be synthesized through various methods, including Friedel-Crafts alkylation. This process involves the introduction of both the tert-butyl and ethoxy groups onto the benzene ring, showcasing the versatility of alkylation reactions in organic synthesis.
  • Applications: This compound is significant in the production of various chemicals. It can be utilized as a solvent or an intermediate in the synthesis of pharmaceuticals and agrochemicals.
  • Research Interest: Chemists are interested in examining the compound due to its potential reactivity and functionalization. The combination of bulkiness and functional groups makes it an excellent candidate for studies focused on reaction mechanisms and catalysis.

As one delves deeper into the world of organic chemistry, compounds like 1-tert-butyl-4-ethoxy-benzene remind us of the intricate balance between structure and reactivity. It is these myriad interactions that make the study of such compounds both challenging and rewarding.

Synonyms
p-tert-Butylphenetole
17269-94-2
Benzene, 1-(1,1-dimethylethyl)-4-ethoxy-
EINECS 241-305-0
DTXSID30169371
1-(1,1-Dimethylethyl)-4-ethoxybenzene
DTXCID9091862
241-305-0
1-tert-Butyl-4-ethoxybenzene
Phenetole, p-tert-butyl-
1-(TERT-BUTYL)-4-ETHOXYBENZENE
ECK6H33VTR
Ethyl 4-terbutylphenyl ether
SCHEMBL635142
SCHEMBL799636
4-Tert-Butylphenyl ethyl ether
SCHEMBL2783422
SCHEMBL3141888
SCHEMBL8140565
SCHEMBL16951860
1-tert-Butyl-4-ethoxybenzene #
AKOS002710535
1-(1,1-dimethylethyl)-4-ethoxy-benzene
NS00025658
InChI=1/C12H18O/c1-5-13-11-8-6-10(7-9-11)12(2,3)4/h6-9H,5H2,1-4H