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4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamide

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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.

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