Triethylamine → HCID 14501040, compound
Reaction equation
[CH3:1][O:2][CH:3]([CH2:15][O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])[CH2:4][S:5]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][OH:14])(=[O:7])=[O:6].C(N(CC)CC)C.[CH3:42][S:43](Cl)(=[O:45])=[O:44]>ClCCl>[CH3:1][O:2][CH:3]([CH2:15][O:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])[CH2:4][S:5]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][O:14][S:43]([CH3:42])(=[O:45])=[O:44])(=[O:7])=[O:6]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In 30 ml of dichloromethane are dissolved 1.77 g of 6-hydroxyhexyl 2-methoxy-3-octadecyloxypropyl sulfone and 0.64 ml of triethylamine, to which 0.35 ml of methanesulfonyl chloride is added dropwise with stirring at room temperature. Thereafter, the mixture is stirred at room temperature for 2 hours and the solvent is distilled off under reduced pressure. The residue is dissolved in ethyl acetate and washed successively with dilute hydrochloric acid, water, an aqueous sodium bicarbonate solution and water. After drying, the solvent is distilled off to leave 1.98 g of the captioned compound.
Workup
- stirringThereafter, the mixture is stirred at room temperature for 2 hours
- distillationthe solvent is distilled off under reduced pressure
- dissolutionThe residue is dissolved in ethyl acetate
- washwashed successively with dilute hydrochloric acid, water
- customAfter drying
- distillationthe solvent is distilled off
Sources & evidence
- ORD record
- ord-c401de8f60d14445989cbae64dc3e275
- Source dataset
- uspto-grants-1989_07
- Patent number
- US04845219
Reaction notes
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