- Product Name:
- Tosylmethyl isocyanide
- Tosylmethy isocyanide ,98%
- Tosylmethyl isocyani
- Isocyanomethyl 4-methylphenyl sulphone
- Toluenesulfonyl Methyl isocyanide
- 4-[(Isocyanomethyl)sulphonyl]toluene, (Toluene-4-sulphonyl)methyl isocyanide
- (p-Tolylsulfonyl)methyl isocyanide, TosMIC, Tosylmethyl isocyanide
- Product Categories:
- Building Blocks
- Chemical Synthesis
- Nitrogen Compounds
- Organic Building Blocks
- Tesaglitazar Carbjdopa
- Sulfur Compounds (for Synthesis)
- Synthetic Organic Chemistry
- Boron, Nitrile, Thio,& TM-Cpds
- Benzene derivatives
- Mol File:
Tosylmethyl isocyanide Chemical Properties
- Melting point:
- 109-113 °C(lit.)
- 1.2721 (rough estimate)
- refractive index
- 1.5270 (estimate)
- storage temp.
- water: slightly soluble
- Water Solubility
- Moisture Sensitive
- CAS DataBase Reference
- 36635-61-7(CAS DataBase Reference)
Tosylmethyl isocyanide Usage And Synthesis
Pale yellow to light brown crystalline powder
Reagent for use in the preparation of biologically active pyrroles and imidazoles.1,2
Tosylmethyl Isocyanide is used as a synthetic reagent in the preparation of variety or biologically active heterocycles such as pyrroles and imidazoles. Tosylmethyl Isocyanide is reported to inhibit [ Fe]-hydrogenase with very high affinity.
Versatile synthon in organic chemistry, especially in the synthesis of heterocyclic Compounds.
A 3-L, three-necked, round-bottomed flask, equipped with a mechanical stirrer, a condenser, and a thermometer, was charged with sodium p-toluenesulfinate 1606 (267 g, 1.5 mol). After the addition of water (750 mL), a 34–37% solution of formaldehyde 1607 (350 mL, 378 g, ca. 4.4 mol), formamide 1608 (600 mL, 680 g, 15 mol), and formic acid (200 mL, 244 g, 5.3 mol), the stirred reaction mixture was heated at 90 C°. The sodium p-toluenesulfinate dissolved during the heating, and the clear solution was kept at 90–95 C° for 2 h. It was then cooled in an ice/salt bath with continued stirring and further cooled overnight in a freezer at 20 C°. The white solid produced was collected by suction filtration. It was washed thoroughly in a beaker by stirring with three 250 mL portions of iced water. The product was dried under reduced pressure over phosphorus pentoxide at 70 C° to provide 134–150 g (42–47%) of crude N-(p-tolylsulfonylmethyl)formamide 1609; mp 106–110 C°. This product was sufficiently pure to be used directly in the following reaction.
Use an efficient fume cupboard. Purify TOSMIC by dissolving (50g) in CH2Cl2 (150mL) and passing it through a column (40x3cm) containing neutral alumina (100g) in CH2Cl2 and eluting with CH2Cl2. A nearly colourless solution (700mL) is collected, evaporated in vacuo and the residue (42-47g) of TOSMIC (m 113-114o dec) is recrystallised once from MeOH (m 116-117o dec). [Hoogenboom et al. Org Synth 57 102 1977, Lensen Tetrahedron Lett 2367 1972.] It also crystallises from EtOH (charcoal) [Saito & Itano, J Chem Soc, Perkin Trans 1 1 1986].
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