Sodium Hydroxide → Thiourea, (2,3-dihydro-1H-inden-2-yl)-
Reaction equation
C([NH:9][C:10]([NH:12][CH:13]1[CH2:21][C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH2:14]1)=[S:11])(=O)C1C=CC=CC=1.[OH-].[Na+]>O>[CH2:14]1[C:15]2[C:20](=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:21][CH:13]1[NH:12][C:10]([NH2:9])=[S:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-Benzoyl-3-(2-indanyl)thiourea (0.931 g.) and sodium hydroxide (0.500 g.) were refluxed in water (6 ml.) for 10 minutes. The mixture was cooled, extracted into chloroform and the chloroform extracts washed with water, dried (MgSO4) and evaporated to give a white solid. Recrystallisation from ethanol/water afforded the title compound as platelets (0.647 g.), m.p. 155.0° C.
Workup
- temperatureThe mixture was cooled
- extractionextracted into chloroform
- washthe chloroform extracts washed with water
- dry with materialdried (MgSO4)
- customevaporated
- customto give a white solid
- customRecrystallisation from ethanol/water
Sources & evidence
- ORD record
- ord-9d356a509a3d42e49cfaea50e67a49e6
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03985898
Reaction notes
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