HCID 70359768, compound → HCID 70359813, compound
Reaction equation
[C:1]1([S:7]([NH:10][CH:11]2[CH2:19][C:18]3[C:13](=[CH:14][CH:15]=[C:16](/[C:20](/[CH3:27])=[CH:21]\[C:22]([O:24]CC)=[O:23])[CH:17]=3)[CH2:12]2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>C(O)C>[C:1]1([S:7]([NH:10][CH:11]2[CH2:19][C:18]3[C:13](=[CH:14][CH:15]=[C:16](/[C:20](/[CH3:27])=[CH:21]\[C:22]([OH:24])=[O:23])[CH:17]=3)[CH2:12]2)(=[O:9])=[O:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
3.4 ml of 15N sodium hydroxide solution are added to 9.1 g (23.6 mmol) of ethyl 3-(2-benzenesulphonamidoindan-5-yl)-crotonate in 100 ml of ethanol and the mixture is boiled for 1 hour. The sodium salt is precipitated on cooling. It is filtered off with suction and dissolved in water. The free acid is precipitated by adding hydrochloric acid and is recrystallised from isopropanol.
Workup
- customThe sodium salt is precipitated
- temperatureon cooling
- filtrationIt is filtered off with suction
- dissolutiondissolved in water
- customThe free acid is precipitated
- additionby adding hydrochloric acid
- customis recrystallised from isopropanol
Sources & evidence
- ORD record
- ord-17d195eed8594025b4a051149a4a9a26
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04929754
Reaction notes
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