While [' 4C-carbonyll -methyl isocyanate has been used widely for the preparation of radioactive insecticidal methylcarbamates, yields are often low, and in some cases reactions completely unsuccessful, because of the sensitivity of the isocyanate to moisture. This paper described a process whereby
A convenient synthesis of [carbonyl-14C]-4-hydroxybenzaldehyde
✍ Scribed by Herbert L. Holland; Nighat Sultana
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 130 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A two‐step synthesis of the title compound from [cyano‐^14^C]‐copper(I) cyanide is described. The method is extensible to the preparation of carbonyl‐labelled 3,4‐dihydroxybenzaldehyde.
📜 SIMILAR VOLUMES
Uniformly ring-14 C]-labelled 4-hydroxybenzaldehyde, vanillin, and protocatechualdehyde were synthesized from [ 14 C]-labelled phenol, guaiacol, and catechol with methyl dichloromethyl sulfide (CH 3 SCHCl 2 ) under Friedel-Crafts alkylation conditions in dichloromethane at À788C for 5 min (in the ca
## Abstract A convenient synthesis with analytical monitoring of ^14^C‐cotinine is reported. ^14^C‐Nicotine was converted into ^14^C‐dibromocotinine hydrobromide perbromide. Debromination, achieved by using Zn dust/acetic acid, resulted in high yields (71%) of ^14^C‐cotinine.
## Abstract A simple and convenient method for the condensation of paminophenol (I) with ^14^C‐acetic anhydride (II) yields up to 76% of ^14^C‐labelled 4‐hydroxyphenylacetamide (carbonyl‐^14^C) (III). Typical synthesis time is 60 minutes. Radioactive yield is 51%, and specific activity is 0.22 μCi/