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Diphenyl carbinol

The spectra and halochromism of thiophene analogs of triphenyl and diphenyl carbinol, " the spectra of anilides of 2- and 3-thenoyl-acetic acid, " and the fluorescence of some thiophene compounds have been investigated. [Pg.19]

The condensation of thiophene with ketones, under the influence of 70% H2SO4, leads to di-2-thienylmethane derivatives. With acetone, 2,2-di-(2-thienyl) propane (97) is obtained. The condensation of thiophene with dimethyl phenyl carbinol, methyl diphenyl carbinol, and f-butylalcohol, in the presence of SnCU gave (98), (99), and 2,5-di-f-butylthiophene, respectively. Triphenyl carbinol does not... [Pg.39]

Allylic and benzylic alcohols were oxidized to aldehydes or ketones with BnPhsPHSOs in refluxing CHsCN. The yield increased in the presence of bismuth chloride in a catalytic amount. Selective oxidation of various alcohols under solvent free conditions was also reported Interestingly, benzyl alcohols were oxidized selectively to benzaldehydes in very high yield (95-100%) when reacted with BnPhsPHSOs (1.2 eq.) and AICI3 (1 eq.) in the presence of an equimolar amount of 2-phenethyl alcohol, diphenyl carbinol or methyl phenyl sulfide (equation 72). [Pg.1031]

Benzyl. pPhenylethyl. Methylphenyl carbinol (1). Ethylphenyl carbinol (2) n Propylphenyl carbinol (3) n-Butylphcnyl carbinol (4). Diphenyl carbinol (5) y-Phenyl-n-propyl (6). Triphenyl carbinol... [Pg.818]

Benzaldehyde and magnesium phenyl bromide or iodide give diphenyl carbinol. [Pg.73]

Bromo-5-nitropyridine gave only the condensation product 301. Bradsher et cyclized the diphenyl carbinol 302 to the 9,9-diphenylpyr-ido[2,l-6]quinazolinium halides 303 by heating in acid. [Pg.343]

Figure 2. Potential fluctuations during the oxidation of diphenyl carbinol (0.1 g Bi/Pi/alumina). Figure 2. Potential fluctuations during the oxidation of diphenyl carbinol (0.1 g Bi/Pi/alumina).
Figure 6. The influence of oxygen partial pressure on the rate of diphenyl carbinol oxidation and on the catalyst potential (0.1 g Bi/Pt/alumina). Figure 6. The influence of oxygen partial pressure on the rate of diphenyl carbinol oxidation and on the catalyst potential (0.1 g Bi/Pt/alumina).
Reaction conditions a-tetralol Diphenyl carbinol 1-phenyl-ethanol... [Pg.383]

Butyl-benzhydryl-ither 6 1386, II633. Athyl-diphenyl-carbinol-ithylithei 6, 687. [Pg.1177]

CaoHuO Cyclohexyl-diphenyl-carbinol-methyh ther 6 II 668. [Pg.2836]

Obtained by reaction of resacetophenone with diphenyl-carbinol in the presence of boron trifluoride etherate in dioxane at r.t. (14%) [3703]. [Pg.1089]

See other pages where Diphenyl carbinol is mentioned: [Pg.818]    [Pg.410]    [Pg.41]    [Pg.818]    [Pg.313]    [Pg.314]    [Pg.371]    [Pg.1031]    [Pg.78]    [Pg.211]    [Pg.108]    [Pg.275]    [Pg.531]    [Pg.663]    [Pg.102]    [Pg.663]    [Pg.100]    [Pg.818]    [Pg.71]    [Pg.59]    [Pg.818]    [Pg.114]    [Pg.381]    [Pg.115]    [Pg.89]    [Pg.71]    [Pg.663]    [Pg.89]    [Pg.1261]    [Pg.2591]    [Pg.2873]   
See also in sourсe #XX -- [ Pg.166 ]



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