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10//- benzothiophene

The presence of thiophene and its derivatives in crude oils was detected in 1899, but until 1953, the date at which the methyl-thiophenes were identified in kerosene from Agha Jari, Iran crude oil, it was believed that they came from the degradation of sulfides during refining operations. Finally, their presence was no longer doubted after the identification of benzothiophenes and their derivatives (Table 8.9), and lately of naphthenobenzothiophenes in heavy cuts. [Pg.324]

The major part of the sulfur contained in crude petroleum is distributed between the heavy cuts and residues (Table 8.10) in the form of sulfur compounds of the naphthenophenanthrene or naphthenoanthracene type, or in the form of benzothiophenes, that is, molecules having one or several naphthenic and aromatic rings that usually contain a single sulfur atom. [Pg.325]

Analogous compounds derived by fusion of a benzene ring to a pyrrole furan or thio phene nucleus are called indole benzofuran and benzothiophene... [Pg.460]

Biological processes are also being studied to investigate abiHty to remove sulfur species in order to remove potential contributors to acid rain (see Air pollution). These species include benzothiophene-type materials, which are the most difficult to remove chemically, as weU as pyritic material. The pyrite may be treated to enhance the abiHty of flotation processes to separate the mineral from the combustible parts of the coal. Genetic engineering (qv) techniques are being appHed to develop more effective species. [Pg.237]

Benzo[b]thiophene-2,3-quinone, 5-chloro-oxidation, 4, 824 Benzothiophenes, 4, 863-934 biological activity, 4, 911-913 intramolecular acylation, 4, 761 mass spectrometry, 4, 739 metabolism, 1, 242 phosphorescence, 4, 16 reactivity, 4, 741-861 spectroscopy, 4, 713-740 structure, 4, 713-740 substituents reactivity, 4, 796-839... [Pg.561]

Thiophene-2-carbaldehyde, 3-bromo-synthesis, 4, 81 Thiophenecarbaldehydes benzothiophene synthesis from, 4, 906 reactions, 4, 807 synthesis, 4, 148 Wittig reactions, 4, 807 Thiophene-2-carb aldehydes bromination, 4, 753 conformation, 4, 33 halogenation, 4, 753 reactions, 4, 72-73 reactivity, 4, 72-73 reduction, 4, 776 Thiophene-3-carb aldehydes conformation, 4, 33 reactivity, 4, 72... [Pg.893]

Thiurets — see 1,2,4-Dithiazolidines, diimino-Thonzylamine antihistamine, 3, 153 Thorpe reaction benzothiophenes from, 4, 876 Thorpe-Ziegler cyclization, 2, 74 Three-membered heterocyclic compounds basicity, 7, 23... [Pg.896]

The only known reaction of a furan with a dihalocarbene is that recently reported between benzofuran and dichlorocarbene in hexane at 0°. The initial adduct (7) could not be isolated but on hydrolysis gave the ring-expanded product 8, possibly via 9, in 15% yield. Benzothiophene was recovered in 92% yield under the same conditions. 2,5-Dihydrofuran reacted with dichloro- and dibromo-carbene to give the products of allylic insertion, 2-dihalogenomethyl-2,5-dihydrofuran, as well as the normal addition products. ... [Pg.64]


See other pages where 10//- benzothiophene is mentioned: [Pg.10]    [Pg.51]    [Pg.77]    [Pg.325]    [Pg.499]    [Pg.460]    [Pg.232]    [Pg.135]    [Pg.9]    [Pg.11]    [Pg.15]    [Pg.16]    [Pg.63]    [Pg.106]    [Pg.109]    [Pg.143]    [Pg.149]    [Pg.151]    [Pg.162]    [Pg.170]    [Pg.142]    [Pg.150]    [Pg.514]    [Pg.561]    [Pg.561]    [Pg.571]    [Pg.572]    [Pg.572]    [Pg.621]    [Pg.703]    [Pg.705]    [Pg.705]    [Pg.62]    [Pg.63]    [Pg.460]    [Pg.65]    [Pg.65]    [Pg.370]   
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1- Benzothiophenes, formation

1- benzothiophene-2-, lithium

1-Benzothiophen

1-Benzothiophen

2-Aryl benzothiophene derivatives

2-Benzothiophen-2,2-dioxid

2-substituted benzothiophenes

4- Amino-benzothiophene

4- Hydroxy-7- benzothiophene

5-substituted benzothiophene

6-Methoxy-2- benzothiophene

Addition to Sulfur in Benzothiophenes

Alkyl benzothiophenes

Annulation with thiophene (synthesis of benzothiophenes)

Aromaticities benzothiophene

Aryl-substituted benzothiophenes

Arylations benzothiophenes

BENZOTHIOPHENE.6(Vol

Benzocyclobutene via thermolysis of benzothiophene dioxides

Benzofuran and Benzothiophene

Benzothieno benzothiophene

Benzothieno benzothiophene synthesis

Benzothieno benzothiophenes

Benzothiophen S-Oxides

Benzothiophen and Dibenzothiophen

Benzothiophene (cont reactions

Benzothiophene 2,2-dioxides, 2,5-dihydrothermolysis benzocyclobutene synthesis

Benzothiophene 5- alkylation

Benzothiophene S -oxidation

Benzothiophene analogs

Benzothiophene analogues

Benzothiophene aromaticity

Benzothiophene carboxamides

Benzothiophene complexes

Benzothiophene coupling reactions

Benzothiophene derivatives

Benzothiophene derivatives, synthesis

Benzothiophene desulfurization

Benzothiophene electron-rich

Benzothiophene halogenation

Benzothiophene hydrogenation

Benzothiophene hydrogenation, homogeneous catalysts

Benzothiophene hydrogenolysis

Benzothiophene mechanisms

Benzothiophene methylation

Benzothiophene nitration

Benzothiophene nucleophilic substitution

Benzothiophene organic sulfur removal

Benzothiophene oxidation sulfoxide

Benzothiophene reactions

Benzothiophene reduction

Benzothiophene ring synthesis

Benzothiophene substrates

Benzothiophene synthesis

Benzothiophene, arylation

Benzothiophene, decomposition

Benzothiophene-1,1-dioxide

Benzothiophene-1,1-dioxide, reduction

Benzothiophene-TCNQ

Benzothiophenes

Benzothiophenes

Benzothiophenes acids/ketones

Benzothiophenes amino

Benzothiophenes and Dibenzothiophenes

Benzothiophenes coupling reactions

Benzothiophenes derivatives

Benzothiophenes design

Benzothiophenes hydrodesulfurization

Benzothiophenes lithiation

Benzothiophenes methylation

Benzothiophenes oxidation

Benzothiophenes reduction

Benzothiophenes ring synthesis

Benzothiophenes structure

Benzothiophenes synthesis

Benzothiophenes, 2,3-dihydroxylation

Benzothiophenes, hydrogenation

Benzothiophenes, nucleophilic substitution

Benzothiophenes, rearrangement

Benzothiophens

Benzothiophens

Benzothiophens and their Benzo-fused Systems

Bonded metal benzothiophene and dibenzothiophene complexes

C-S bond cleavages of thiophenes, benzothiophenes, and dibenzothiophenes

Catalysts benzothiophene

Electron-rich benzothiophenes

Furans, Benzofurans, Thiophenes, and Benzothiophenes

Furo benzothiophenes

Fused benzothiophenes

Halo-benzothiophenes

Heteroaryl Heck reaction benzothiophene

Hydrogenation of benzothiophenes

Hydrogenolysis of benzothiophenes

Indole, Benzofuran, and Benzothiophene

Indoles, benzofurans and benzothiophenes

Ionic hydrogenation benzothiophenes

Oxidation benzothiophene

Oxidative desulfurization benzothiophene

Reactions of Thiophene and Benzothiophene

Reactions with Thiophene and Benzothiophene

Selenolo benzothiophenes

Synthesis of Benzothiophenes

Synthesis of Benzothiophenes and Benzofurans

Synthesis of Benzothiophenes via 4 1 Cycloaddition Reactions

Synthesis of Benzothiophens

Synthesis of Benzothiophens by Ring-closure Reactions

Synthesis of Thiophene and Benzothiophene

Tetracyclic benzothiophenes

Thianaphthene (2,3-Benzothiophene)

Thieno benzothiophene

Thieno benzothiophenes

Thiophene benzothiophenes

Thiophenes and benzothiophenes

Thiophens and Benzothiophens

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