A convenient synthesis of trifluoromethyl aryl sulfides
✍ Scribed by Béatrice Quiclet-Sire; Radomir N. Saicic; Samir Z. Zard
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 122 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Trifluoromethyl aryl sulfides are obtained in moderate/good yields by heating potassium trifluoroacetate and aryl disulfides in sulfolane Copyright © 1996 Elsevier Science Ltd
Trifluoromethyl aryl sulfides are important intermediates in the preparation of biologically active compounds, l dyes, 2 and useful chemical reagents. 3 So far, compounds of this type have been obtained mainly by multi-step procedures involving chlorination of methyl aryl sulfides followed by chloride/fluoride exchange;4, 5 however, o-substituted derivatives cannot be obtained in this way. More direct methods for the
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The fractional distillation of 0-(2-alkenyl or 2-cycloalkenyl) S-alkyl dithiocarbonates (xanthates) affords 2-alkenyl or 2-cycloalkenyl alk'yl