Sodium Hydroxide → HCID 14819408, compound
Reaction equation
[CH3:1][C:2]1([CH3:22])[CH:11](O)[CH:10]([S:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:20]#[N:21])[CH:8]=2)[CH2:3]1.[OH-].[Na+]>O1CCOCC1>[CH3:1][C:2]1([CH3:22])[CH:11]=[C:10]([S:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:20]#[N:21])[CH:8]=2)[CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 1 g of 2,2-dimethyl-4-(2-pyridylthio)-6-cyano-1,2,3,4-tetrahydro-3-naphthol, 0.3 g of NaOH and 35 ml of dioxane is boiled for 20 minutes. The mixture is cooled and filtered and the filtrate is evaporated and worked up in the customary manner to give 2,2-dimethyl-4-(2-pyridylthio)-6-cyano-1,2-dihydronaphthalene.
Workup
- temperatureThe mixture is cooled
- filtrationfiltered
- customthe filtrate is evaporated
Sources & evidence
- ORD record
- ord-25203165af634dc2b4c73a5529abdfec
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05132307
Reaction notes
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