Potassium Hydroxide → HCID 54563878, compound
Reaction equation
C12(C([O:13][C:14]3[CH:15]=[C:16]4[C:21](=[CH:22][CH:23]=3)[O:20][C:19]([C:24]35C[CH:28]6[CH2:29][CH:30]([CH2:32][CH:26]([CH2:27]6)[CH2:25]3)C5)=[CH:18][C:17]4=[O:34])=O)CC3CC(CC(C3)C1)C2.[OH-].[K+]>O1CCOCC1>[OH:13][C:14]1[CH:15]=[C:16]2[C:21](=[CH:22][CH:23]=1)[O:20][C:19]([CH:24]=[CH:25][C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:32]=1)=[CH:18][C:17]2=[O:34]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
330 mg 6-(1-adamantoyloxy)-2-(1-adamantyl)-4H-chromen-4-one is dissolved in dioxane and treated with 5 ml of 10% aqueous potassium hydroxide solution. The mixture is stirred for 3 hours at room temperature and then poured into 2M aqueous pH 7 buffer solution. Extraction with ethyl acetate yields after drying and evaporation a crude product which is purified by chromatogaphy. The title compound is obtained [colourless crystals; mp 230°(from 2-propanol)].
Workup
- extractionExtraction with ethyl acetate
- customyields
- customafter drying
- customevaporation a crude product which
- customis purified by chromatogaphy
Sources & evidence
- ORD record
- ord-f5948e2dae9f47e9b039a3e1b0ba51d5
- Source dataset
- uspto-grants-2002_02
- Patent number
- US06346626B1
Reaction notes
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