ChemicalBook > Product Catalog > Organic Chemistry > Amides > 4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamide
4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamide
4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamide Basic information
- Product Name:
- 4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamide
- Synonyms:
-
- BenzenesulfonaMide, 4-Methyl-N-2-propyn-1-yl-
- 4-methyl-N-prop-2-ynylbenzenesulfonamide
- 4-methyl-N-(prop-2-yn-1-yl)benzenesulfonamide
- 4-methyl-N-(prop-2-yn-1-yl)benzene-1-sulfonamide
- 4-METHYL-N-(2-PROPYNYL)BENZENESULFONAMIDE
- CAS:
- 55022-46-3
- MF:
- C10H11NO2S
- MW:
- 209.26
- Mol File:
- 55022-46-3.mol
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4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamide Chemical Properties
- Melting point:
- 76 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
- Boiling point:
- 333.4±52.0 °C(Predicted)
- Density
- 1.209±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C, stored under nitrogen
- pka
- 9.43±0.50(Predicted)
- Appearance
- White to off-white Solid
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4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamide Usage And Synthesis
Synthesis
Add triethylamine (9.5 mL, 70 mmol, 1.4 equivalents), followed by tosyl chloride (9.53 g) portionwise to a stirred solution of propargylamine (3.84 mL, 60 mmol) in dry dichloromethane (50 mL, 1.2 M) at 0°C under argon atmosphere. Stir the mixture overnight at room temperature. Add water (50 mL) to the mixture. Extract the aqueous layer by dichloromethane (2 × 50 mL). Dry the combined organic layers over MgSO4. Concentrate the combined organic layers under reduced pressure.
References
[1]Bodinier, Florent et al. Low-valent dialkoxytitanium(ii): a useful tool for the synthesis of functionalized seven-membered ring compounds†.”Chemical Communications 29 (2021): 3603–3606.
4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamideSupplier
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