Sodium Chloride → HCID 20075700, compound
Reaction equation
[CH2:1]([SH:3])[CH3:2].[CH2:4]([CH:9]1[CH2:14][CH2:13][CH:12]([CH:15]2[CH2:20][CH2:19][C:18]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])(O)[CH2:17][CH2:16]2)[CH2:11][CH2:10]1)[CH2:5][CH2:6][CH2:7][CH3:8].C(OC(=O)C)(=O)C.Cl(O)(=O)(=O)=O.[Cl-].[Na+]>C(O)(=O)C>[CH2:4]([CH:9]1[CH2:14][CH2:13][CH:12]([CH:15]2[CH2:20][CH2:19][C:18]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])([S:3][CH2:1][CH3:2])[CH2:17][CH2:16]2)[CH2:11][CH2:10]1)[CH2:5][CH2:6][CH2:7][CH3:8]Participants
7
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
7.2 g of ethanethiol and 35 g of 4-pentyl-4'heptyl-4'-hydroxybicyclohexane in 70 ml of glacial acetic acid are added dropwise to a mixture of 30 ml of glacial acetic acid, 11.1 g of acetic anhydride and 7 g of 72% aqueous perchloric acid solution at -20°. The mixture is stirred at room temperature for 24 hours, poured into 250 ml of saturated sodium chloride solution, extracted with petroleum ether and worked up in the customary manner. 4-Pentyl-4'-heptyl-4'-ethylthiobicyclohexane is obtained.
Workup
- extractionextracted with petroleum ether
Sources & evidence
- ORD record
- ord-0469ec7d524d4eeabe5d4242ea5d8e13
- Source dataset
- uspto-grants-1991_01
- Patent number
- US04985583
Reaction notes
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