Triethylamine → HCID 22902165, compound
Reaction equation
[C:1]([NH:5][CH3:6])([CH3:4])([CH3:3])[CH3:2].C(N(CC)CC)C.[Cl:14][CH2:15][CH2:16][CH2:17][S:18](Cl)(=[O:20])=[O:19]>ClCCl>[C:1]([N:5]([CH3:6])[S:18]([CH2:17][CH2:16][CH2:15][Cl:14])(=[O:20])=[O:19])([CH3:4])([CH3:3])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
1.74 g(0.02 mol) of t-butylmethylamine and 2 equivalents of triethylamine were dissolved in 100 ml of dichloromethane, which was stirred at 0° C. 3.54 g(0.02 mol) of 3-chloropropane sulfonyl chloride dissolved in 50 ml. of dichloromethane was added dropwise and the mixture was stirred for 1 hour at room temperature. The organic layer was washed with 1N HCl aqueous solution and dried over MgSO4 to obtain 3.31 g of the title compound(yield 73%).
Workup
- stirringthe mixture was stirred for 1 hour at room temperature
- washThe organic layer was washed with 1N HCl aqueous solution
- dry with materialdried over MgSO4
Sources & evidence
- ORD record
- ord-8eab1a3579404059bab5076a1408fc45
- Source dataset
- uspto-grants-1997_10
- Patent number
- US05679687
Reaction notes
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