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![Technical Aspect of the Automated Synthesis and Real-Time Kinetic Evaluation of [11C]SNAP-7941](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59557.jpg&w=3840&q=50)
Technical Aspect of the Automated Synthesis and Real-Time Kinetic Evaluation of [11C]SNAP-7941
Published on: April 28, 2019
A facile synthesis of [(11)C]acetylene
Rachid Nazih1, Jeremy P Blauser, Bruce H Mock
1Department of Radiology, Indiana University School of Medicine, 1345 W. 16th Street L-3 R# 204, Indianapolis, IN 46202, USA.
Abstract:
Acetylene is a versatile synthon organic chemistry. The complexity and difficulty of synthesis of [(11)C]acetylene has limited its use as a labeling intermediate for PET radiotracers. A new method for production of [(11)C]acetylene has been developed in our laboratory that simplifies the synthesis procedure allowing for easy automation and implementation. The technique is a modification of Madsen et al. (1981, Phys. Med. Biol. 26(5), 875) that utilized carbon dioxide ((11)C) and barium. First [(11/12)C]CO(2) was trapped at room temperature on barium within a quartz reaction tube, then heated to 900 degrees C under hydrogen flow to release [(11)C]acetylene. Hydrogen gas is apparently oxidized to form water vapor which reacts immediately with the formed carbide to liberate acetylene. Radiochemical yields of 31.4--75.4% and specific activities of 0.11-- 161 mCi/micromol have been obtained with radiochemical purities greater than 99%. This technique provides a new, efficient and very practical synthesis of [(11)C]acetylene that can be utilized as synthon for novel PET radiopharmaceuticals.
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The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.

