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T-butyl mercaptan

Scheme 5-5. Reagents and conditions a NaOCE Ph, THF/DMF 5 1, — 10°C to room temperature, b LiAlELt, Et20, reflux, c AC2O, Py. d (1) Cat. RuCh/NaKTt, CCI4/ MeCN/H20 1 1 1.5, room temperature. (2) LiOH, THF/H20 5 4, 0°C. (3) 2N HC1, Et20, 0°C to room temperature, e (1) IV-methylmorpholine, isobutylchloroformate, N-hydroxy-2-thiopyridone, THF, NEt3, TFIF, — 15°C, (2) t-butyl mercaptan, irradiation, THF, room temperature, f H2, 10% Pd/C, EtOFI. g Cat. ( -Pr)4NRu04, NMO, 4 A MS, CH2CI2, room temperature. Scheme 5-5. Reagents and conditions a NaOCE Ph, THF/DMF 5 1, — 10°C to room temperature, b LiAlELt, Et20, reflux, c AC2O, Py. d (1) Cat. RuCh/NaKTt, CCI4/ MeCN/H20 1 1 1.5, room temperature. (2) LiOH, THF/H20 5 4, 0°C. (3) 2N HC1, Et20, 0°C to room temperature, e (1) IV-methylmorpholine, isobutylchloroformate, N-hydroxy-2-thiopyridone, THF, NEt3, TFIF, — 15°C, (2) t-butyl mercaptan, irradiation, THF, room temperature, f H2, 10% Pd/C, EtOFI. g Cat. ( -Pr)4NRu04, NMO, 4 A MS, CH2CI2, room temperature.
Other Derivatives of Isobutylene. The production of many smaller-volume chemicals is based on high-purity isobutylene. The major chemicals are para-t-butylphenol, di-t-butyl-p-cresol (butylated hydroxytoluene, BHT), 2,6-di-t-butylphenol, t-butylamine, t-butyl mercaptan, and isobutyl aluminum compounds. Isobutylene usage by each of these six ranged from 8 to 18 million lb. The total volume of isobutylene that went for small-volume chemical production was about 140 million lb in 1997. [Pg.389]

The N-hydroxypyridine-2-thione esters of Boc-protected amino acids undergo decarboxylation on photolysis in the presence of a hydrogen-atom-transfer reagent such as t-butyl mercaptan in 80-95% yield. Decarboxylation of the side-chain carboxy groups of suitably protected aspartic and glutamic acids can also be effected, but yields are lower (50-80%). ... [Pg.417]

Methyl hydrazine Methyl isobutyl ketone Methyl isobutyrate Methyl, mercaptan Methyl methacrylate 1 -Methylnaphthalene 2-Methyl-2-propanethiol, see t-Butyl mercaptan Methyl-n-Propyl ketone 1 -Methylpyrrole Methyl salicylate a-Methyl styrene m.-p-Methyl styrene Methyl sulphate, see Dimethyl sulphate... [Pg.120]

Sauers, R. R., Van Arnum, S. D. A Thio-Staudinger Reaction Thermolysis of a Vinyl Azide in the Presence of t-Butyl Mercaptan. Phosphorus, Sulfur Silicon Relat. Elem. 2003, 178, 2169-2181. [Pg.684]

Di-t-butyl disulfide 423 Isobutene, isobutane, t-butyl mercaptan, (Fe-S)... [Pg.266]

Beilstein Handbook Reference) BRN 0505947 EINECS 200-890-2 HSDB 1611 t-Butyl mercaptan tert-Butanethiol tert-Butyl mercaptan tert-Butylthiol tertiary-Butyl mercaptan. Has skunk-like odor. Used as additive to natural gas for leak detection. Liquid mp = -0.5° bp = 64.3° d = 0.7943 soluble in organic solvents, insoluble in H2O. Lancaster Synthesis Co. Mallinckrodt Inc. Sigma-Aldrich Fine Chem. [Pg.95]

Selective reduction of aldehydes. An aldehyde group can be reduced selectively in the presence of a ketone group by NaBHi in the presence of an added thiol (ethyl mercaptan, t-butyl mercaptan see 6, 532). [Pg.534]

The final unequivocal experimental proof that the observed effects were indeed peripheral ones was obtained in psychophysical experiments. Tertiary butyl mercaptan was used as the target in a monorhinal presentation. Its perceived odor intensity remained unchanged when in a dichorhinal experiment the contralateral na-ris was exposed to a very low Intensity of l -cyclohexyl-l -methyl-2-pentanone (CMP, 13). However, in agreement with established crossover additivity, the total perceived overall odor intensity showed a small, but statistically significant increase. Then the two separate odorant streams of the dichorhinal experiment were combined and the mixture of malodor (t.-butyl mercaptan) and AMAL (CMP) presented to the subjects again. Perceived overall intensity was reduced by and perceived malodor intensity by 85 at a significance level of 5%. [Pg.173]

N-Benzyldimethylamine Benzyltriethyl ammonium chloride Benzyl trimethyl ammonium chloride Bis (2-ethylhexyl) maleate Bis (glycidoxypropyl) tetramethyidisiloxane 3-[Bis (2-hydroxyethyl) amino] propyltriethoxysilane N,N -Bis (2-hydroxypropyl)-2-methylpiperazine Bis-(N-methylbenzamide) ethoxymethyl silane Bisphenol A ethoxylate diacrylate Bis-(3-(triethoxysilyl) propyl) tetrasulfane Bis (trimethoxysilylpropyl) ethylene diamine Bis (trimethylsilyl) urea 1-Butoxyethoxy-2-propanol Butoxytriglycol t-Butyl alcohol n-Butyl chloroformate n-Butyldimethylchlorosilane Butyl lactate t-Butyl mercaptan Butyl myristate t-Butyl perbenzoate Butyl sulfide Calcium undecylenate C8-10 alcohols C14-15 alcohols... [Pg.5386]

Captan Ethyl sulfide Isopropyl mercaptan odorant, gas leak detection t-Butyl mercaptan... [Pg.5487]

Fig. 2. Hammett equation plot of relative k. values vs. Fig. 2. Hammett equation plot of relative k. values vs. <r constants. For each system, k,/k is plotted, where k is the intercept of the least-squares line for that system system I, 0.1 M azoisobutane (AIB) and thiophenol-d system II, 0.1 M t-butyl peroxypivalate (BPP) and thiophenol-d system III, 0.1 M AIB and t-butyl mercaptan-d [73 Pry 2].
Treatment of the o-chlorobenzylamine derivative (333) with potassium amide in liquid ammonia yields, inter alia, the isoindole (334) by benzyne cyclization. The stable fluorescent isoindole (335) is formed from phthalaldehyde, t-butyl mercaptans, and propylamine. The base-induced elimination of methanesul-phinic acid from compound (336) affords the bis-isoindole (337) the benzo[l,2-f> 4,5-c ]dipyrrole (338) has been prepared in two steps from 5,6-dibenzoyl- 1 -methylindole. ... [Pg.44]


See other pages where T-butyl mercaptan is mentioned: [Pg.211]    [Pg.120]    [Pg.127]    [Pg.447]    [Pg.434]    [Pg.311]    [Pg.118]    [Pg.266]    [Pg.95]    [Pg.414]    [Pg.688]    [Pg.95]    [Pg.631]    [Pg.4883]    [Pg.6057]    [Pg.6703]    [Pg.7034]    [Pg.507]    [Pg.340]    [Pg.10]    [Pg.11]    [Pg.385]    [Pg.535]    [Pg.298]    [Pg.523]    [Pg.534]    [Pg.845]    [Pg.908]    [Pg.1340]   


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