Sodium Hydroxide → Sodium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenylpropionate
Reaction equation
[C:1]12([C:11]([O:13][CH:14]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:15]([C:18]([O:20]CC)=[O:19])([F:17])[F:16])=[O:12])[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.O1CCOCC1.[OH-].[Na+:36]>O>[C:1]12([C:11]([O:13][CH:14]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:15]([F:16])([F:17])[C:18]([O-:20])=[O:19])=[O:12])[CH2:8][CH:7]3[CH2:9][CH:3]([CH2:4][CH:5]([CH2:6]3)[CH2:10]1)[CH2:2]2.[Na+:36]Participants
Procedure
A mixture of 6.6 g of 2-ethoxycarbonyl-2,2-difluoro-1-phenylethyl 1-adamantanecarboxylate, prepared in Synthesis Example 1-5, 20 g of 1,4-dioxane, and 2.5 g of 25 wt % sodium hydroxide was stirred for 2 hours. Water, 30 g, was added to the reaction solution. The reaction solution was washed with n-hexane, obtaining an aqueous solution of sodium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenylpropionate. To this solution, 32 g of an aqueous solution of triphenylsulfonium chloride and 100 g of methylene chloride were added. After stirring for 30 minutes, the organic layer was taken out, washed with water, and concentrated under reduced pressure. Methyl isobutyl ketone was added to the concentrate, which was concentrated again. Diisopropyl ether was added to the concentrate for crystallization. The resulting solid was dried in vacuum, obtaining 5.5 g of the target compound, triphenylsulfonium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenylpropionate as white crystals (yield 58%).
Workup
- washThe reaction solution was washed with n-hexane
Sources & evidence
- ORD record
- ord-e3b0863aa0444ee68115008ade79ec4d
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221742B2
Reaction notes
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