## Abstract The synthesis of the __d__~4~‐forms of __rac__‐ and __R__‐lofexidine was accomplished. Two methods are described; one method is a two‐step synthesis of __rac__‐__d__~4~‐lofexidine from 2‐chloropropionitrile, the second method is a three‐step preparation of __R__‐__d__~4~‐lofexidine in a
Synthesis of [4″-3H]- and [4,4,5,5-2H4]-2-(1′-[2′,6″-Dichlorophenoxy]-ethyl)-Δ2-imidazoline
✍ Scribed by Gerd Kloster; Johannes Odenthal
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 205 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
[4″‐^3^H]‐2‐(1‐[2″,6″‐Dichlorophenoxy]‐ethyl‐Δ^2^‐imidazoline) was prepared from [4‐^3^H]‐2,6‐dichlorophenol in two different ways. By reaction of 2,6‐dichlorophenol with 2‐(α‐chloroethyl)‐Δ^2^‐imidazoline, the radiochemical yield, at a specific activity of 173.9 mCi/mmole, was 12.8 %. With the two‐step‐procedure (reaction of 2,6‐dichlorophenol with 1.) 2‐chloropropionitrile and 2. ethylenediamine, the radiochemical yield of product, at a specific activity of 185.8 mCi/mmole, was 30.0 %.
[4,4,5,5‐^2^H~4~]‐2‐(1′‐[2″,6″‐Dichlorophenoxy]‐ethyl)‐Δ^2^‐imidazoline was prepared in one step from [1,1,2,2‐^2^H~4~]‐ethylene‐diamine in 49 % yield.
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## Abstract 1,1,1‐Trifluoroalkane‐2,3‐dione 3‐oximes 1 easily obtainable from aldehyde dimethylhydrazones were reacted with several aldehydes and ketones in the presence of acetic acid to afford 4‐trifluoromethyl‐4__H__‐[1,5,2]dioxadines 3 in satisfactory yields. When the reaction was carried out i
## Abstract Starting from commercially available [2,3,4,5,6‐^2^H~5~]benzoic acid, [2,3,4,5,6‐^2^H~5~]phenyl glucosinolate was synthesized. Under negative‐ion electrospray‐ionization mass spectrometric conditions, this compound affords a peak at __m__/__z__ 399. Since this __m__/__z__ value is not k