1980
DOI: 10.1002/chin.198026168
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ChemInform Abstract: SYNTHESIS OF NEW BIS(P‐CHLOROPHENYLTHIO)‐ AND BIS(P‐CHLOROPHENYLSULFONYL)METHANES

Abstract: Die aliphatischen bzw. aromatischen Aldehyde (I) werden mit dem Thiophenol (II) zu den Thioacetalen (IIIa) bzw. (IIIb) kondensiert; ebenso werden in einer Variante dieser Reaktion aus den Ketonen (IV) die Thioketale (V) synthetisiert.

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“…Yield: 114 mg (63%); a pale yellow oil. 1,1-Di(4-chlorophenylthio)ethane (4) 29 Yield: 53 mg (34%); a pale yellow oil. 1,1-Bis(benzylthio)ethane (7) 26 Yield: 71 mg (52%); a pale yellow oil 1,1-Bis(butylthio)ethane (8) 30 Yield: 60 mg (58%); a pale yellow oil.…”
Section: 1-di(4-tert-butylphenylthio)ethane (3) 28mentioning
confidence: 99%
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“…Yield: 114 mg (63%); a pale yellow oil. 1,1-Di(4-chlorophenylthio)ethane (4) 29 Yield: 53 mg (34%); a pale yellow oil. 1,1-Bis(benzylthio)ethane (7) 26 Yield: 71 mg (52%); a pale yellow oil 1,1-Bis(butylthio)ethane (8) 30 Yield: 60 mg (58%); a pale yellow oil.…”
Section: 1-di(4-tert-butylphenylthio)ethane (3) 28mentioning
confidence: 99%
“…1,1-Di(4-tert-butylphenylthio)ethane (3) 28 Yield: 114 mg (63%); pale yellow oil. 1,1-Di(4-chlorophenylthio)ethane (4) 29 Yield: 53 mg (34%); pale yellow oil. 1 H NMR (500 MHz, CDCl 3 ):  = 7.39 (d, J = 8.5 Hz, 4 H, C 6 H 4 ), 7.29 (d, J = 8.5 Hz, 4 H, C 6 H 4 ), 4.46 (q, J = 6.8 Hz, 1 H, CH), 1.58 (d, J = 7.0 Hz, 3 H, CH 3 ).…”
Section: 1-di(4-methylphenylthio)ethane (1) 26mentioning
confidence: 99%