Thionyl Chloride (SOCl2)

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Conductivity of Thionyl Chloride-Lithium Tetrachloroaluminate Solutions

The specific conductivity of solutions of LiA1C14 dissolved in SOC12 was determined as a function of composition and temperature. An analytical expression from which the conductivity can be calculated is given as a function of the mole fraction of LiA1C14 and temperature in the ranges from 0 ~ to 0.37~ and from -20 ~ to +70~ respectively. LiAIC14-SOC14 mixtures are used commercially as electrol...

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C1 Nuclear Quadrupole Interaction in Thionyl Chloride

21 hyperfine multiplets, up to J = 12, have been measured for thionyl chloride (S0C12), by means of microwave spectroscopy in the region 18.0 —26.5 GHz. Nuclear quadrupole coupling constants along the principal axes of inertia were determined to be Xaa ~ ~ 25.004 ± 0.040 MHz, Xbb = 0.009 ± 0.025 MHz and Xce = 25.013 ± 0.031 MHz. Also, coupling constants along the S—CI bond axis (z axis) and two...

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Chlorination of (Phebox)Ir(mesityl)(OAc) by Thionyl Chloride.

Pincer (Phebox)Ir(mesityl)(OAc) (2) (Phebox = 3,5-dimethylphenyl-2,6-bis(oxazolinyl)) complex, formed by benzylic C-H activation of mesitylene (1,3,5-trimethylbenzene) using (Phebox)Ir(OAc)2OH2 (1), was treated with thionyl chloride to rapidly form 1-(chloromethyl)-3,5-dimethylbenzene in 50% yield at 23 °C. A green species was obtained at the end of reaction, which decomposed during flash colum...

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On the reaction of anthranilic acid with thionyl chloride : Iminoketene intermediate formation

It has been reported that sulfinamide anhydride is formed when anthranilic acid is treated with thionyl chloride under anhydrous conditions. Garin et al. reported that no sulfinamide anhydride was formed in the reaction of anthranilic acid with thionyl chloride. They reported that 2-(sulfinylamino) benzoyl chloride was formed, in accordance with an earlier observation, under the same reaction c...

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thionyl chloride (or oxalyl chloride) as an efficient acid activator for one-pot synthesis of β-lactams

thionyl chloride (or oxalyl chloride) has been used as an efficient and cheap acid activator for one-pot synthesis of β-lactams in good to excellent yields by reaction between imines and acids in the presence of triethylamine at room temperature.

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ژورنال

عنوان ژورنال: Journal of Synthetic Organic Chemistry, Japan

سال: 1983

ISSN: 0037-9980,1883-6526

DOI: 10.5059/yukigoseikyokaishi.41.1110