## Abstract The synthesis of 1‐fluoro‐4,4‐di‐hydroxymethyl‐pentane (I) and its dicarbamate (II) is described. (I) is obtained by classical alkylation of methylmalonic ester with 1‐ bromo‐3‐fluoro‐propane and subsequent reduction with LiAlH~4~, of the fluorinated diester obtained. Treated with phosg
Recherches sur la formation et la transformation de dérivés organiques du fluor V. Synthèse de quelques esters du diéthylamino-1-fluoro-3-propanol-2
✍ Scribed by Emile Cherbuliez; A. Yazgi; J. Rabinowitz
- Publisher
- John Wiley and Sons
- Year
- 1960
- Tongue
- German
- Weight
- 302 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The synthesis of some esters of 1‐diethylamino‐3‐fluoro‐propan‐2‐olis described. The nitrobenzoic ester is transformed with very good yield into the corresponding aminobenzoic ester by reduction with Sn and HC1 or by catalytic hydrogenation.
📜 SIMILAR VOLUMES
3,3‐dimethylpentane‐2,4‐diol, a new diol, and its dicarbamate have been prepared. Some N,N‐diethylcarbamates of diols have also been prepared from N,N‐diethylcarbamoyl chloride and the corresponding diols.
Some new diethylcarbamates of dialkylamino‐alcohols of type I (fluorinated or not) have been prepared from diethylcarbamylchloride and the corresponding aminoalcohols.
## Abstract Some new fluorinated hydroxy‐acids and hydroxy‐ethers as well as their phosphorylated derivatives are described.
## Abstract On décrit la synthèse, en quatre étapes a partir de l'acide dibromo‐ 4, 6‐isophtalique, de dérivés di‐ et tétraméthylés du cis‐fluorbnackne ([indéno‐2′, 1′: 2,3‐fluorkne]). Ce sont le diméthyl‐3,6‐cis‐fluorknacbne ou diméthyl‐6,6′‐[indho‐2′, 1′ : 2,3‐fluorène], le téraméhyl‐1, 3,6,8‐ ci