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Hexahydrobenzo

Cyclohexylcarbinol has been prepared by the reduction of ethyl hexahydrobenzoate with sodium and alcohol, and by... [Pg.24]

On hydrogenation, delphinine forms hexahydrodelphinine, CgaHgjOgN, m.p. 192-3°, by reduction of the benzoyl radical, hexahydrobenzoic acid replacing benzoic acid as a product of hydrolysis. [Pg.697]

Reaction of trans-1,2-cyclohexanediol with para-formaldehyde in the presence of Indion 130 as catalyst to yield the corresponding cyclic formal has been successfully carried out (Matkar and Sharma, 1995). A conversion of 52% was realized with 70% selectivity towards cyclohexanediol formal the other side products are rrans-hexahydrobenzo-l,3,5-trioxypin, di(tra i -2-hydroxycyclo-hexyloxy) methane. [Pg.131]

Hexahydrobenzene, c347 Hexahydrobenzoic acid, c353 Hexahydrobenzylamine, c362 Hexahydrophthalic acid, c356 Hexahydropyridine, pi80 Hexamethylenediamine, h53 Hexamethylene diisocyanate, d461... [Pg.235]

XIX), methyl 2-fluoromethyl-3 6-endomethylene-A -tetrahydro-benzoate (XX) and methyl 2 fluoromethyl 3 6 endomethylene hexahydrobenzoate (XXI). [Pg.172]

Uses Manufacture of adipic acid, hexahydrobenzoic acid, maleic acid, 1,3-butadiene catalyst solvent oil extraction component of coal tar stabilizer for high octane gasoline organic synthesis. [Pg.337]

Dihydrobenzopyran (chromane) and its methyl homologs were reduced by lithium in ethylamine and dimethylamine to 3,4,5,6,7,8-hexahydrobenzo-pyrans in 84.5% yields [424. ... [Pg.53]

Hydrogenation over nickel catalyst at high temperatures and pressures affects aromatic rings. Over Urushibara nickel at 106-150° and 54atm, ethyl benzoate gave ethyl hexahydrobenzoate in 82% yield [48]. [Pg.156]

Estradiol, 161 Estradiol benzoate, 162 Estradiol cypionate, 162 Estradiol dipropionate, 162 Estradiol hexahydrobenzoate, 162 Estradiol valerate, 162 Estrogenic activity, 100 Estrogens, 100, 160 antagonists,104 discovery, 155 impeded, 104 Estrone, 156, 161... [Pg.481]

The enamine-immonium cation system of 9,10-dimethoxy-l,2,3,4-6,7-hexahydrobenzo[a]quinolizinium salt [166]. [Pg.64]

The cis and trans isomers of ethyl-2,3-dihydrobenzo[i>]thiophen-2,3-ylene acetate (30)228 and cis -and fr]thiophene 27 have been synthesized. Addition of chlorine to the 5,6-double bond of 31 affords a mixture of cis- and[Pg.206]

When 3-mercaptocyclohexanone condenses with dichloroacet-aldehyde or chloroacetaldehyde in the presence of a catalytic quantity of acid (e.g., p-toluenesulfonic acid), simultaneous cyclization occurs to give 4,5,6,7-tetrahydrobenzo[6]thiophen-4-one (see Section VI, B, 4) and 2,4,5,6,7,7a-hexahydrobenzo[6]thiophen-4-one (see Section... [Pg.210]

By the same general method, M-butyl bromide gives m-valeric acid in 64-65 per cent yield, bromobenzene gives benzoic acid in 70-71 per cent yield, and cyclohexyl bromide gives hexahydrobenzoic acid in 68 per cent yield. [Pg.77]

Hexahydrobenzoic acid, c317 Hexahydrobenzylamine, c324 Hexahydrophthalic acid, c320 Hexahydropyridine, pi 83 Hexamethylenediamine, h56 Hexamethylene diisocyanate, d410... [Pg.261]

Irradiation of 720a in MeOH saturated with 2-butyne affords 2,3-dihy-drothiophene-3-acetate 721, 3-thiabicyclo[3.1.0]hexane 722, and 2,3-dihy-drothiophene-3-carboxylate 723 in a 1 1 1 ratio. From 720b, a 1 1 mixture of trans-fused 3a,4,5,6,7,7a-hexahydrobenzo[b]thiophene 724 and of 2,3-dihy-drothiophene-3-carboxylate 725 is formed. [Pg.351]

Taira, K. Lai, K. Gorenstein, D. G. Stereoelec-tronic effects in the conformation and hydrolysis of epimeric (4aa, 8a/ )-hexahydrobenzo-2-(p-nitrophenoxy)-2-oxo-l,3,22.5dioxaphosphori-... [Pg.33]

The synthesis of S-keto-hexahydrobenzoic acid further illustrates the use of cyanacetic ester,17... [Pg.14]

Similar results were obtained with enamines of acyclic ketones such as desoxybenzoin. Nitrostyrene gave only the less substituted mono-alkylated enamine and hence the / -nitro-a-phenylethyl ketone on hydrolysis117. Surprisingly 2-nitropropene gives mainly the tetrasubstituted cyclohexanone enamine106. A hexahydrobenzo-l,2-oxazine-7V-oxide (55) was isolated at low temperatures (in 80% yield) which rearranged at room temperature to a mixture of alkylated enamine isomers107 (Scheme 39). [Pg.757]


See other pages where Hexahydrobenzo is mentioned: [Pg.789]    [Pg.789]    [Pg.62]    [Pg.699]    [Pg.162]    [Pg.442]    [Pg.789]    [Pg.789]    [Pg.177]    [Pg.98]    [Pg.331]    [Pg.331]    [Pg.461]    [Pg.213]    [Pg.789]    [Pg.789]    [Pg.240]    [Pg.256]    [Pg.365]    [Pg.2015]    [Pg.65]    [Pg.542]    [Pg.48]    [Pg.55]    [Pg.221]   


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Ethyl hexahydrobenzoate

Hexahydrobenzoic acid

Methyl 2.fluoromethyl-3:6-endomethylene hexahydrobenzoate

Methyl hexahydrobenzoate

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