IX.—The Synthesis of 8-Bromo-3-methoxyfluoranthene.

Author(s):  
Neil Campbell ◽  
Naim M. Hasan

SummaryA second method for the synthesis of 8-bromo-3-methoxyfluoranthene from 2-bromo-7-methoxyfluorene is described. The autoxidation of fluorene derivatives including the 9-carboxylic acids and of related compounds, particularly 4-α-cyanobenzyl-7−oxo-7H-benz[de]anthracene, is discussed. Unsuccessful attempts to prepare 3-bromofluorene-9-acetic acid in good yield are reported.

1983 ◽  
Vol 61 (10) ◽  
pp. 2423-2424 ◽  
Author(s):  
Suzanne R. Abrams

Substituted acetic acids can be prepared in good yield (50–80%) from terminal acetylenes of the same chain length. The alkyne is first converted to the thiophenyl ether, which is treated without purification with mercuric sulfate in acetic acid and 2 N sulfuric acid affording the carboxylic acid. The method is particularly useful in the synthesis of long chain ω-hydroxyalkanoic acids.


2018 ◽  
Vol 16 (1) ◽  
pp. 34-39
Author(s):  
Yao-Wei Li ◽  
Pei-Ming Zhang ◽  
Rui Li ◽  
Yan Bai ◽  
Yu Yu ◽  
...  

CDI combined with CH3SO3H was found to be highly effective for the cyclization of 2-aminothiophenol derivatives with carboxylic acids under MW condition. Fourteen benzothiazole derivatives were synthesized in good yield and their structures were characterized by 1H-NMR, 13CNMR, IR and mass spectrometry. This simple, rapid synthetic method is believed to provide a useful process for the synthesis of 2-substituted benzothiazole compounds.


1974 ◽  
Vol 27 (10) ◽  
pp. 2205 ◽  
Author(s):  
T Fujita ◽  
S Watanabe ◽  
K Suga

Lithium naphthalenide reacts with carboxylic acids in the presence of diethylamine to give the α-anions of lithium carboxylates. Reaction of these anions with various epoxides gives the corresponding y-hydroxy acids in good yield. The γ-hydroxy acids easily cyclize to give γ-butyrolactones.


1987 ◽  
Vol 40 (10) ◽  
pp. 1663 ◽  
Author(s):  
J Rosevear ◽  
JFK Wilshire

The reaction of several substituted o- nitronitrosobenzenes with O- and p- anisidine , and 2,4- dimethoxyaniline in acetic acid gives in good yield the corresponding enitroazobenzenes which are readily reduced with thiourea dioxide ( formamidinesulfinic acid) to the corresponding 2-(methoxypheny1)-2H-benzotriazoles, demethylation of which furnished the corresponding 2- (hydroxypheny1)-2H-benzotriazoles. Demethylation of the dimethoxy derivatives was best accomplished with boron tribromide in methylene chloride, the methoxy group located ortho to the benzotriazole ring being demethylated more readily than is the para-methoxy group. The reaction of enitroazobenzenes containing a methoxy group with hydrobromic acid in acetic acid results in cleavage of the azo bond and also partial bromination to give o- nitroaniline and some of its brominated derivatives.


2013 ◽  
Vol 78 (14) ◽  
pp. 7216-7222 ◽  
Author(s):  
Tomonori Iitsuka ◽  
Petra Schaal ◽  
Koji Hirano ◽  
Tetsuya Satoh ◽  
Carsten Bolm ◽  
...  

1988 ◽  
Vol 22 (12) ◽  
pp. 2841-2850 ◽  
Author(s):  
H. Puxbaum ◽  
C. Rosenberg ◽  
M. Gregori ◽  
C. Lanzerstorfer ◽  
E. Ober ◽  
...  

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