## Abstract [5‐^14^C]‐Dodecane and [8‐^14^C]‐Hexadecane were synthesized starting with [1‐^14^C]‐octanoic acid. The carboxylic acid was reduced to 1‐octanol, which was esterified to n‐octyl p‐toluenesulfonate. Following a Corey‐House procedure, the sulfonate was either reacted with Li[Cu(butyl)~2~]
Synthesis of 3-(hydroxymethyl-14C)-8-methoxychromone-214C and 3-hydroxymethyl–8-methoxychromone-4-14C
✍ Scribed by E. J. Merrill; A. D. Lewis
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- French
- Weight
- 311 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A simple route to 3‐(hydroxymethyl‐^14^C)‐8‐methoxychromone‐2‐^14^ using formaldehyde‐^14^C is described. However, this material was considered to be unacceptable for most biological studies because about 16% of the radioactivity was expired as ^14^CO~2~ in the mouse. The synthesis of 3‐methoxysalicylic (carboxyl‐^14^C) acid is described which was converted in several steps to 3‐hydroxymethyl‐8‐methoxychromone‐4‐^14^C. Only 0.03% of the radioactivity in this compound was expired as ^14^CO~2~.
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