HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506739Generated: October 29, 2026
Hydrochloric Acid → Ethyl difluoro-(2-hydroxy-adamantan-2-yl)acetate
https://huagongshe.com/reaction/1506739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Adamantanone | HCID 64151 | — |
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl difluoro-(2-hydroxy-adamantan-2-yl)acetate | HCID 117966647 | 58% |
Reaction Steps
A mixture of 24 g of ethyl bromodifluoroacetate, 2.2 g of dibromoethane and 25 g of tetrahydrofuran was added dropwise to a mixture of 7.8 g of zinc, 15 g of 2-adamantanone, 30 mL of trimethyl borate, and 25 g of tetrahydrofuran at a temperature of 50° C., followed by stirring for 10 hours at 80° C. Thereafter, 50 g of 5 wt % hydrochloric acid was added to quench the reaction. Ethyl acetate, 20 g, was added to the reaction solution, from which the organic layer was extracted. The organic layer was washed with saturated sodium chloride water and then with water. The reaction solution after washing was concentrated under reduced pressure. Methyl isobutyl ketone was added to the concentrate, the resulting solution was concentrated under reduced pressure again, and n-hexane was added to the concentrate for crystallization. The resulting solid was dried in vacuum, obtaining 15 g of the target compound, ethyl difluoro-(2-hydroxyadamantan-2-yl)acetate 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-132195967112493698db12b11b48dcb5 |
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| Source note | uspto-grants-2015_12 |
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