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Updated: May 20, 2026
![Microwave-assisted One-pot Synthesis of N-succinimidyl-4-[18F]fluorobenzoate ([18F]SFB)](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F2755.jpg&w=3840&q=50)
Microwave-assisted One-pot Synthesis of N-succinimidyl-4-[18F]fluorobenzoate ([18F]SFB)
Published on: June 28, 2011
2-[2-(3-Methyl-but-oxy)-5-nitro-benz-amido]-acetic acid dimethyl sulfoxide monosolvate
Abstract:
In the title compound, C(14)H(18)N(2)O(6)·C(2)H(6)OS, the -C(O)NHCH(2)CO(2)H and -O(CH(2))(2)CH(CH(3))(2) substitutents of the aromatic ring are positioned such that the -NH- group is hydrogen-bond donor to the ether O atom of the other substituent. The dimethyl sulfoxide solvent mol-ecule is linked to the carb-oxy-lic acid group by an O-H⋯O hydrogen bond.
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Nomenclature of Carboxylic Acid Derivatives: Acid Halides, Esters, and Acid Anhydrides
The IUPAC and common names of acid halides are derived from the corresponding carboxylic acids, by changing “ic acid” to “yl halide.” For example, as shown below, the IUPAC name ethanoyl chloride is derived from ethanoic acid, and the common name, acetyl chloride, is obtained from acetic acid.

