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Synthesis of (1-/sup 11/C)-butanol

Abstract

A method for carrier-free labelling of n-butanol with the positron emitting radionuclide carbon-11 (half-life 20.4 min) is described. Labelling was achieved by carboxylation of n-propyl magnesium chloride with /sup 11/C-labelled carbon dioxide and the subsequent reduction of the resulting free (1-/sup 11/C)-butyric acid with LiAlH/sub 4/ after hydrolysis of the Grignard complex. The procedure permits /sup 11/C-labelled butanol to be prepared in high activity and high radiochemical purity for in vivo biological studies only 25 min after the start of carboxylation of the Grignard compound. Gas chromatography and HPLC were used to assess the purity of the product. To maintain carrier-free conditions, atmospheric carbon dioxide was rigorously excluded from all reagents and every parts of the apparatus.
Authors:
Oberdorfer, F; Helus, F; Maier-Borst, W; [1]  Silvester, D J [2] 
  1. Deutsches Krebsforschungszentrum, Heidelberg (Germany, F.R.)
  2. Hammersmith Hospital, London (UK). M.R.C. Cyclotron Unit
Publication Date:
Sep 20, 1982
Product Type:
Journal Article
Reference Number:
AIX-14-741030; EDB-83-096479
Resource Relation:
Journal Name: Radiochem. Radioanal. Lett.; (Switzerland); Journal Volume: 53:4; Other Information: 8 refs
Subject:
38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEAR CHEMISTRY; 62 RADIOLOGY AND NUCLEAR MEDICINE; BUTANOLS; LABELLING; CARBON 11; RADIOCHEMISTRY; RADIOPHARMACEUTICALS; CHEMICAL PREPARATION; ALUMINIUM HYDRIDES; BUTYRIC ACID; CARBON DIOXIDE; CARBOXYLATION; FLOWSHEETS; GAS CHROMATOGRAPHY; GRIGNARD REAGENTS; HALF-LIFE; IMPURITIES; LABORATORY EQUIPMENT; LIQUID COLUMN CHROMATOGRAPHY; LITHIUM HYDRIDES; MAGNESIUM CHLORIDES; NITROGEN 14 TARGET; TRAPPED PROTONS; TRAPS; ALCOHOLS; ALKALI METAL COMPOUNDS; ALKALINE EARTH METAL COMPOUNDS; ALUMINIUM COMPOUNDS; BARYONS; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; CARBON COMPOUNDS; CARBON ISOTOPES; CARBON OXIDES; CARBOXYLIC ACIDS; CHALCOGENIDES; CHEMICAL REACTIONS; CHEMISTRY; CHLORIDES; CHLORINE COMPOUNDS; CHROMATOGRAPHY; DIAGRAMS; DRUGS; ELEMENTARY PARTICLES; EQUIPMENT; EVEN-ODD NUCLEI; FERMIONS; HADRONS; HALIDES; HALOGEN COMPOUNDS; HYDRIDES; HYDROGEN COMPOUNDS; HYDROXY COMPOUNDS; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; LITHIUM COMPOUNDS; MAGNESIUM COMPOUNDS; MINUTES LIVING RADIOISOTOPES; MONOCARBOXYLIC ACIDS; NUCLEI; NUCLEONS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANOMETALLIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PROTONS; RADIOISOTOPES; SEPARATION PROCESSES; SYNTHESIS; TARGETS; 400702* - Radiochemistry & Nuclear Chemistry- Properties of Radioactive Materials; 550601 - Medicine- Unsealed Radionuclides in Diagnostics
OSTI ID:
6346950
Country of Origin:
Switzerland
Language:
English
Other Identifying Numbers:
Journal ID: CODEN: RRALA
Submitting Site:
HEDB
Size:
Pages: 237-252
Announcement Date:
Mar 01, 1983

Citation Formats

Oberdorfer, F, Helus, F, Maier-Borst, W, and Silvester, D J. Synthesis of (1-/sup 11/C)-butanol. Switzerland: N. p., 1982. Web.
Oberdorfer, F, Helus, F, Maier-Borst, W, & Silvester, D J. Synthesis of (1-/sup 11/C)-butanol. Switzerland.
Oberdorfer, F, Helus, F, Maier-Borst, W, and Silvester, D J. 1982. "Synthesis of (1-/sup 11/C)-butanol." Switzerland.
@misc{etde_6346950,
title = {Synthesis of (1-/sup 11/C)-butanol}
author = {Oberdorfer, F, Helus, F, Maier-Borst, W, and Silvester, D J}
abstractNote = {A method for carrier-free labelling of n-butanol with the positron emitting radionuclide carbon-11 (half-life 20.4 min) is described. Labelling was achieved by carboxylation of n-propyl magnesium chloride with /sup 11/C-labelled carbon dioxide and the subsequent reduction of the resulting free (1-/sup 11/C)-butyric acid with LiAlH/sub 4/ after hydrolysis of the Grignard complex. The procedure permits /sup 11/C-labelled butanol to be prepared in high activity and high radiochemical purity for in vivo biological studies only 25 min after the start of carboxylation of the Grignard compound. Gas chromatography and HPLC were used to assess the purity of the product. To maintain carrier-free conditions, atmospheric carbon dioxide was rigorously excluded from all reagents and every parts of the apparatus.}
journal = []
volume = {53:4}
journal type = {AC}
place = {Switzerland}
year = {1982}
month = {Sep}
}