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phenyl(phenylsulphonyl)trimethylsilylmethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91787-22-3

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91787-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91787-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91787-22:
(7*9)+(6*1)+(5*7)+(4*8)+(3*7)+(2*2)+(1*2)=163
163 % 10 = 3
So 91787-22-3 is a valid CAS Registry Number.

91787-22-3Relevant academic research and scientific papers

Double elimination protocol for the synthesis of arylene ethynylenes containing heteroaromatic rings

Orita, Akihiro,Ye, Fangguo,Babu, Govindarajulu,Ikemoto, Tomohiro,Otera, Junzo

, p. 716 - 727 (2007/10/03)

The double elimination reaction of β-substituted sulfones offers a versatile strategy for synthesis of arylene ethynylene kits containing heteroaromatic rings. A sequence of aldol reaction between α-sulfonyl carbanion and aldehyde, trapping the resulting aldolate to give β-substituted sulfone, and double elimination of this intermediate can be integrated in one pot. This protocol allows thiophene, pyridine, and ferrocene units to be accommodated in phenylene ethynylene arrays.

Automated synthesis: Utilization of MEDLEY in synthetic processes

Orita, Akihiro,Yasui, Yutaka,Otera, Junzo

, p. 337 - 341 (2013/08/07)

A variety of reactions which are commonly used in synthetic chemistry are feasible with the automated synthesizer (MEDLEY). Air-sensitive organolithium and Grignard reagents as well as transition metal catalysts like Ni(0) and Pd(0) species are employable. The precise control of both the reaction temperature and the amount of added reagents enables to examine the dependence of chemical yields on the reaction temperature. Since the order of reagent addition is programmed and the reaction temperature is quickly tunable, sequential reactions can be conducted smoothly. An advanced control system was incorporated which allows a task to start immediately after the preceding one has finished. Owing to this function, the time for completing the multistep process can be minimized.

Integrated Chemical Process: One-Pot Double Elimination Method for Acetylenes

Orita, Akihiro,Yoshioka, Naonori,Struwe, Petra,Braier, Arnold,Beckmann, Anke,Otera, Junzo

, p. 1355 - 1363 (2007/10/03)

A novel one-pot process for synthesis of acetylenes has been achieved in which the following series of steps are integrated: addition of an α-anion of sulfone to aldehyde; trapping of the resulting adduct to incorporate a leaving group, and double elimination of this intermediate. Consolidation of Peterson elimination renders the process much simpler. This method provides a convenient and high-yielding access to a variety of enynes and polyynes as well as to functionally substituted aryl acetylenes containing halogen(s) or acetal groups, which are useful building blocks for aryl acetylene scaffolds. Iteration of the one-pot generation of acetylenic bonds provides a new metodology for the buildup of aryl acetylene skeletons.

Integrated chemical process. One-pot preparation of acetylenes by Peterson-sulfone elimination

Orita, Akihiro,Yoshioka, Naonori,Otera, Junzo

, p. 1023 - 1024 (2007/10/03)

Integration of silylation of α-sulfonyl carbanion, addition of the anion of the resulting α-silyl sulfone to aldehyde, Peterson elimination, and sulfone elimination leads to one-pot synthesis of acetylenes.

The Synthesis of Ketones via α-Silyl Sulphides

Ager, David J.

, p. 195 - 204 (2007/10/02)

α-Phenylthiosilanes (2) have been prepared by alkylation of the anion (4) derived from the 1-phenylthio-1-trimethylsilylalkane (1).These anions (4) have benn prepared by a variety of methods including, direct deprotonation of (1), displacement of a phenylthio group by lithium naphthalenide addition of an alkyl-lithium to 1-phenylthio-1-trimethylsilylethene (7), and transmetallation of a tributylstannyl moiety.The formation of an alkyl-lithium by reaction of lithium naphthalenide with a phenyl sulphide provided an additional route to (2) from bis(phenylthio)acetals (8).An alternative path to the α-phenylthiosilanes (2) was to reduce the corresponding α-phenylsulphonylsilane (15); these, in turn, being readily available from alkylation or silylation of α-sulphonyl anions.The α-phenylthiosilanes (2) were converted into the O-trimethylsilylphenylthioacetal (18) by the sila-Pummerer rearrangement, although this was complicated by vinyl sulphide (20) formation in certain cases.Subsequent hydrolysis of (18) and (20) gave the ketone (3).

Preparation of sulfines by alkylidenation of sulfur dioxide using α-silyl carbanions

Porskamp, P. A. T. W.,Leij, M. van der,Lammerink, B. H. M.,Zwanenburg, B.

, p. 400 - 404 (2007/10/02)

The synthesis of sulfines 4 from a series of active methylene compounds is described.Deprotonation, followed by silylation, gives the trimethylsilyl compounds 2.Subsequent deprotonation to α-silyl carbanions and treatment with an excess of sulfur dioxide

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