Water → HCID 15052910, compound
Reaction equation
[C:1]1([S:7]([NH:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]#N)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH2:21].[OH-:22].[Na+]>C(O)C>[C:1]1([S:7]([NH:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]([OH:22])=[O:21])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
9-(Benzenesulphonamido)nonanenitrile (0.72 g) was dissolved in ethanol (50 ml) and water (10 ml) containing sodium hydroxide (1.5 g). The mixture was refluxed for 18 hours then the solvent was removed. The residue was dissolved in water and treated with hydrochloric acid to give a white precipitate. This was collected by filtration and recrystallised from methanol-water to give the title compound (0.52 g) m.p. 82°-84° C.
Workup
- temperatureThe mixture was refluxed for 18 hours
- customthe solvent was removed
- dissolutionThe residue was dissolved in water
- additiontreated with hydrochloric acid
- customto give a white precipitate
- filtrationThis was collected by filtration
- customrecrystallised from methanol-water
Sources & evidence
- ORD record
- ord-46979f2e90bc4a3d8778c7ca047cdc0e
- Source dataset
- uspto-grants-1991_03
- Patent number
- US04997847
Reaction notes
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