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Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH. It is a colourless liquid with a pleasant floral odor. It occurs widely in nature, being found in a variety of essential oils. It is slightly soluble in water (2 ml per 100 ml of H 2 O), but miscible with most organic solvents.
Phenethyl acetate is the ester resulting from the condensation of acetic acid and phenethyl alcohol. Like many esters, it is found in a range of fruits and biological products. [1] It is a colorless liquid with a rose and honey scent and a raspberry-like taste. [2] [3]
However, this synthesis risks the self-condensation of alcohol itself (e.g. ethanol self-condenses to form diethyl ether). A more common and higher-yielding reaction is the Williamson ether synthesis , where a phenol is converted by a strong base to the phenoxide ion, which can subsequently be reacted with an alkyl halide via nucleophilic ...
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4-EP is biosynthesized in two steps from p-coumaric acid.Decarboxylation gives 4-vinylphenol as catalyzed by the enzyme cinnamate decarboxylase. [4] 4-Vinylphenol is further reduced to 4-ethylphenol by the enzyme vinyl phenol reductase.
Ethyl butyrate, also known as ethyl butanoate, or butyric ether, is an ester with the chemical formula CH 3 CH 2 CH 2 COOCH 2 CH 3. It is soluble in propylene glycol, paraffin oil, and kerosene. It has a fruity odor, similar to pineapple, and is a key ingredient used as a flavor enhancer in processed orange juices. [1]
The reaction of acetophenone enolate with phenyl isothiocyanate. In this one-pot synthesis [9] the ultimate reaction product is a Thiazolidine. This reaction is stereoselective with the formation of the Z-isomer only. Electrochemical reduction gives thioformamides. [10]: 340
1-Phenylethanol is the organic compound with the formula C 6 H 5 CH(OH)CH 3.It is one of the most commonly available chiral alcohols. It is a colorless liquid with a mild gardenia-hyacinth scent.