Sodium 4-hydroxybenzenesulfonate → HCID 22645035, compound
Reaction equation
[Na+].[OH:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([O-:12])(=[O:11])=[O:10])=[CH:5][CH:4]=1.Br[CH2:14][C:15]#[C:16][C:17]1[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][CH:18]=1>C(O)(C)C.[OH-].[Na+]>[Cl:23][C:20]1[CH:21]=[CH:22][C:17]([C:16]#[C:15][CH2:14][O:2][C:3]2[CH:8]=[CH:7][C:6]([S:9]([OH:12])(=[O:10])=[O:11])=[CH:5][CH:4]=2)=[CH:18][CH:19]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 70 °C
Procedure
To a solution of 4-hydroxybenzenesulfonic acid sodium salt (2.81 g, 12.11 mmol) in 50 mL of isopropyl alcohol, 11.8 mL 2N NaOH and 5.56 g (24.2 mmol, 2 eq) of 1-(3-bromo-prop-1-ynyl)-4-chloro-benzene was added. The solution was heated to 70° C. overnight. The reaction was cooled, concentrated in vacuo, filtered and air dried to afford 2.8 g (67%) of 4-[3-(4-chloro-phenyl)-prop-2-ynyloxy]-benzenesulfonic acid, sodium salt. Electrospray Mass Spec 321.3 (M−H)−
Workup
- temperatureThe reaction was cooled
- concentrationconcentrated in vacuo
- filtrationfiltered
- customair dried
Sources & evidence
- ORD record
- ord-674b335b714647d68daf0ad43f8fb4bf
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06225311B1
Reaction notes
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