Hydrochloric Acid → HCID 13785667, compound
Reaction equation
[Cl:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5](C2C=CC=CC=2S([O-])(=O)=O)=[C:4]([CH3:21])[CH:3]=1.[OH-:22].[Na+].Cl>O>[Cl:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([OH:22])=[C:4]([CH3:21])[CH:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
84.2 (0.26 mol) of the ester from step 2 are suspended in 1 l of water and mixed with 30.8 g (0.77 mol) of sodium hydroxide platelets. After 2 hours cooking under reflux the starting material is cooled and the solution is adjusted to a pH value of 2.1 with 2 N hydrochloric acid. The precipitated material is filtered by suction, washed with water and dried in vacuum at 50° C. The yield amounts to about 45.6 g 95.4% of the theoretical yield).
Workup
- temperatureunder reflux the starting material
- temperatureis cooled
- filtrationThe precipitated material is filtered by suction
- washwashed with water
- customdried in vacuum at 50° C
- customtheoretical yield)
Sources & evidence
- ORD record
- ord-1bc42961b19f41b284e79ae10e8a600c
- Source dataset
- uspto-grants-1990_10
- Patent number
- US04960955
Reaction notes
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