HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369907Generated: October 29, 2026
Water → (2R)-2-[(1R)-3,3-difluorocyclopentyl]-2-hydroxy-2-phenylacetic acid
https://huagongshe.com/reaction/369907
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Pyridine, hydrofluoride (1:1) | HCID 64774 | — |
| Reactant | Nitrilooxonium tetrafluoroborate | HCID 11137142 | — |
| Reactant | (2R,5R)-2-(t-butyl)-5-((1R)-3-hydroxyiminocyclopentyl)-5-phenyl-1,3-dioxolan-4-one | HCID 86754451 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2R)-2-[(1R)-3,3-difluorocyclopentyl]-2-hydroxy-2-phenylacetic acid | HCID 10890505 | — |
Reaction Steps
To a suspension of 20 mg of nitrosonium tetrafluoroborate in 0.5 ml of 70% hydrogen fluoride-pyridine, a solution of 34 mg of (2R,5R)-2-(t-butyl)-5-((1R)-3-hydroxyiminocyclopentyl)-5-phenyl-1,3-dioxolan-4-one in 0.5 ml of dichloromethane was added under cooling with ice, followed by stirring for 10 minutes at 0° C. and for 5 hours at room temperature. Water was added to the reaction mixture under cooling with ice, and extraction was carried out with ethyl acetate. After sequential washing with a saturated aqueous solution of sodium hydrogencarbonate and brine, the organic layer was dried over anhydrous magnesium sulfate. Distilling the solvent off under reduced pressure gave 35 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06140333 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-a5627e87915e4aac8f46ff7e9149549d |
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| Source note | uspto-grants-2000_10 |
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