Benzoyl peroxide Benzylic

Benzidine-based dyes Benzo Azurine G Benzo(a)fluoranthene Benzo(b)fluoranthene Benzo(j)fluoranthene Benzo(k)fluoranthene Benzo(g,h,i)perylene Benzopurpurine 4B Benzo(a)pyrene Benzo(c) pyrene Benzo(e) pyrene Benzosulphonazole Benzothiazole Benzoyl peroxide Benzyl chloride Beryllium... [Pg.365]

Benzotrichloride (see also a-Chlorinated toluenes and benzoyl chloride) Benzoyl chloride (see also a-Chlorinated toluenes and benzoyl chloride) Benzoyl peroxide Benzyl acetate... [Pg.534]

Benzidine (based dyes) Benzo(a)pyrene Benzoyl peroxide Benzyl chloride Beryllium and compounds Biphenyl Bismuth lelluride Borates, lelra, sodium salts Boron oxide... [Pg.408]

Benzidine Benzoic trichloride (Benzotrichloride) Benzoyl chloride Benzoyl peroxide Benzyl chloride Beryllium Biphenyl... [Pg.59]

Juenge3 has now found that the reagent is effective for nuclear or side-chain halogenation of aromatic systems, the former occurring under ionic conditions, the latter under free-radical conditions. Thus benzene and naphthalene are chlorinated under Lewis acid catalysis 1 -chloronaphthalene can be prepared in 58% yield. Toluene under similar conditions gives a mixture of 2- and 4-chloro-toluene in 66% yield. In the presence of benzoyl peroxide, benzyl chloride is obtained in 44% yield. [Pg.354]

A few typical medicinal compounds that are prepared hy the aforesaid henzoylation methods shall he discussed explicitely in the sections that follow, namely Benzoyl Glycine N-Benzoyl- 3-Alanine Flavone Benzoyl Peroxide Benzyl henzoate. [Pg.93]

Aluminum acetate Aluminum caprylate Aluminum distearate Aluminum myristates/palmitates Aluminum stearate Aluminum tristearate N-2-Aminoethyl-3-aminopropyl trimethoxysilane Aminoethylethanolamine Aminomethyl propanol Aminopropyltriethoxysilane Aminopropyltrimethoxysilane Ammonium benzoate Ammonium borate Ammonium citrate dibasic Ammonium laureth sulfate Ammonium laureth-5 sulfate Ammonium laureth-7 sulfate Ammonium laureth-12 sulfate Ammonium laureth-30 sulfate Ammonium lauryl sulfate Ammonium maleic anhydride/diisobutylene copolymer Ammonium oleate Ammonium persulfate Ammonium polyacrylate Ammonium potassium hydrogen phosphate Ammonium stearate Ammonium sulfamate Ammonium thiocyanate Ammonium thiosulfate Amyl acetate Antimony trioxide Asbestos Asphalt Azelaic acid 2,2 -Azobisisobutyronitrile Barium acetate Barium peroxide Barium sulfatej Bentonite Benzalkonium chloride Benzene Benzethonium chloride Benzothiazyl disulfide Benzoyl peroxide Benzyl alcohol Benzyl benzoate 1,3-Bis (2-benzothiazolylmercaptomethyl) urea 1,2-Bis (3,5-di-t-butyl-4-hydroxyhydrocinnamoyl) hydrazine 4,4 -Bis (a,a-dimethylbenzyl) diphenylamine Bisphenol A Bis (trichloromethyl) sulfone Boric acid 2-Bromo-2-nitropropane-1,3-diol 1,4-Butanediol Butoxydiglycol Butoxyethanol Butoxyethanol acetate n-Butyl acetate Butyl acetyl ricinoleate Butyl alcohol Butyl benzoate Butyl benzyl phthalate Butyidecyl phthalate Butylene glycol t-Butyl hydroperoxide... [Pg.4796]

L-Ascorbic acid Benzoic acid Benzoyl peroxide Benzyl alcohol Benzylparaben BHA BHT Biphenyl Boric acid t-Butyl hydroquinone... [Pg.5565]

Trivial name Acetaldehyde Acetamide Acetic acid Acetic anhydride Acetoacetic acid Acetone Acetonitrile Acetophenone Acetyl chloride Acetylene Acrolein Acrylamide Acrylic acid Acrylonitrile Adipic acid Amyl acetate Amyl alcohol tert-Amy alcohol Aniline Azelaic acid Benzoic acid Benzoyl peroxide Benzyl alcohol Bisphenol A... [Pg.282]

Polycarbonate 1 Benzoyl Peroxide Benzyl Octyl Adipate ... [Pg.3375]

Side-chain bromination at the benzylic position occurs when an alkylbenzene is treated with /V-bromosuccinimide (NBS). For example, propylbenzene gives (l-bromopropyl)benzene in 97% yield on reaction tvith NBS in the presence of benzoyl peroxide, (PhC02)2f as a radical initiator. Bromination occurs exclusively in the benzylic position and does not give a mixture of products. [Pg.578]

Avramoff et al. have already reported that the reaction of hydrocarbons such as toluene with tetramethylammonium tribromide (TMA Br3) in benzene, in the presence of benzoyl peroxide at room temperature gave benzylic bromination products (ref. 21). However, TMA Br3 is not easy to handle in comparison with the stable BTMA Br3 because of its hydroscopic character. Furthermore, as shown in their literature, a large excess of TMA Br3 is necessary to brominate arenes. [Pg.37]

BENZOYLINDOLE, 56, 8 Benzoyl peroxide, 56, 50 58, 80, 82 3-Benzoylpropionitrile, 59, 56 Benzyl alcohol, 59, 3 Benzylamine-polystyrene, 56, 95 Af-Benylbenzamide, 59, 52 l-Benzyl-2-benzoyl-l,2-dihydroisoquin-... [Pg.112]

N -Fmoc serine benzyl ester 2, which could be prepared as shown or purchased commercially, was smoothly converted to the crystalHne O-methylthiomethyl (MTM) ether 3 in high yield via a Pummerer-Hke reaction using benzoyl peroxide and dimethyl sulfide in acetonitrile [39]. This common intermediate was used to synthesize both 5 and 8 [40]. Both Ogilvie [41] and Tsantrizos [42] had reported that I2 was an effective activator with similar MTM ether substrates. The H promoted nucleosidation reaction between O-MTM ether 3 and bis-silylated thymine 4 produced the nucleoamino acid 5 in 60% isolated yield (100% based on recovered 3). Hydrogenolytic deprotection of the benzyl ester with H2, Pd/C in MeOH gave the thymine-containing nucleoamino acid 6 in quantitative yield. [Pg.200]

Benzophenone, 46, 36 N-(2-Benzothiazolyl)urea, 46, 72 Benzoyl chloride, reaction with hydrogen fluoride, 46, 4 Benzoyl fluoride, 46, 3 Benzoylhydrazine, 46, 8S Benzoyl peroxide, reaction with diethyl ethylmalonate, 45, 37 2-Benzyl-2-carbomethoxycyclopenta-none, 45, 7... [Pg.57]

Biuret triisocyanate-adduct of hexamethylene diisocya- Mobay Chem. Co. nate with water Dibutyltin dilaurate Dimethyl 2,5-bis(ethyl-hexanoyl peroxy)hexane Benzoyl peroxide Calcium naphthenate Lead naphthenate Cobalt naphthenate Zinc naphthenate N-benzyl-N,N,dimethylamine Copper chloride Ferric chloride N,N-(Dimethylaminoethyl)-morpholine -Caprolactone Hydorquinone Xylene... [Pg.299]

The synthesis of anastrozole (Scheme 3.3) began with an 8 2 displacement of commercially available 3,5-fc (bromomethyl)toluene (19) using potassium nitrile and a phase-transfer catalyst, tetrabutylammonium bromide (Edwards and Large, 1990). The resulting fcw-nitrile 20 in DMF was then deprotonated with sodium hydride in the presence of excess methyl iodide to give the fc -dimethylated product 21. Subsequently, a Wohl-Ziegler reaction on 21 was carried out using A-bromosuccinamide (NBS), and a catalytic amount of benzoyl peroxide (BPO) as the radical initiator. Finally, an Sn2 displacement of benzyl bromide 22 with sodium triazole in DMF afforded anastrozole (2) as a white solid. [Pg.36]

Beckmann rearrangement of, 729,741 p-Benzoquinone, 745 Benzoylacetone, 865 o-Benzoylbenzoic acid, 728, 739 Benzoyl chloride, 791, 792 Benzoyl glycine, 584 Benzoyl peroxide, 807 determination of, 809 Benzoyl piperidine, 489, 492 P-Benzoylpropionic acid, 728, 737 P-Benzoylpropionitrfle, 911, 912 Benzoyl-p-toluidide, 582, 583 Benzyl acetate, 780, 783 Benzylacetophenone, 726, 734 Benzyl alcohol, 706,711, 811,812,884 N-Benzylamid es 394 table of, 395 ... [Pg.1169]

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