Hydrochloric Acid → HCID 21404070, compound
Reaction equation
[OH-].[K+].C([O:6][C:7]1[C:16]([S:17]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36])=[O:18])=[CH:15][C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=1)(=O)C.Cl>C(O)C>[CH2:19]([S:17]([C:16]1[C:7]([OH:6])=[CH:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[CH:11][CH:10]=2)=[O:18])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 25 g potassium hydroxide in 500 ml ethanol was added 25 g (0.051 mole) 3-octadecanesulfinyl-2-naphthyl acetate. The mixture was stirred at room temperature in a nitrogen atmosphere for 1.5 hr. then acidified with 5% hydrochloric acid. The solid was collected, dried, and recrystallized from hexane-ethyl acetate to give 17 g of light pink solid, m.p. 107°-108° C.
Workup
- customThe solid was collected
- customdried
- customrecrystallized from hexane-ethyl acetate
Sources & evidence
- ORD record
- ord-201c6bb4f36b45f0acc5a37cd6b51346
- Source dataset
- uspto-grants-1977_10
- Patent number
- US04053312
Reaction notes
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