HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506738Generated: October 27, 2026
Sodium Hydroxide → Sodium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenylpropionate
https://huagongshe.com/reaction/1506738
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, which was washed with n-hexane, obtaining an aqueous solution of sodium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenylpropionate. To this solution, 95 g of an aqueous solution of 4-tert-butylphenyldiphenylsulfonium methylsulfate 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 5.4 g of the target compound, 4-tert-butylphenyldiphenylsulfonium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenylpropionate as white crystals (yield 52%).
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-4e4840187ebc4f069741026905ed7138 |
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| Source note | uspto-grants-2015_12 |
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