HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506737Generated: October 27, 2026
Sodium Hydroxide → Sodium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenylpropionate
https://huagongshe.com/reaction/1506737
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Ethoxycarbonyl-2,2-difluoro-1-phenylethyl 1-adamantanecarboxylate | HCID 117966692 | — |
| Solvent | Water | HCID 962 | — |
| Product | Sodium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenylpropionate | HCID 117966807 | — |
Reaction Steps
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%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221742B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-e3b0863aa0444ee68115008ade79ec4d |
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| Source note | uspto-grants-2015_12 |
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