HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731001Generated: October 30, 2026
Water → 1-Chloro-2-(2,4-difluorophenyl)butane-2,3-diol
https://huagongshe.com/reaction/731001
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 1-Chloro-2-(2,4-difluorophenyl)-3-(tert-butyldimethylsilyloxy)butan-2-ol | HCID 23117047 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Chloro-2-(2,4-difluorophenyl)butane-2,3-diol | HCID 23117040 | 17% |
Reaction Steps
To a solution of 0.27 g (0.77 mmol) of 1-chloro-2-(2,4-difluorophenyl)-3-(tert-butyldimethylsilyloxy)butan-2-ol ((2S,3R)/(2R,3R)=91/9) in 3 mL of methanol was added 0.06 g (0.94 mmol) of potassium fluoride, and reaction was performed for 10 hours and then at 50° C. for another 25 hours. Next, 5 mL of water was added to stop the reaction, and extraction was performed with 10 mL of ethyl acetate. The resulting organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain a crude product as a colorless oil. The resulting crude product was quantitatively analyzed by HPLC (under the same HPLC measurement conditions as those in Example 6). Thereby, the title compound was obtained in a yield of 17% ((2S,3R)/(2R,3R)=95/5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582781B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-a125feee18d0457d957eda867789655c |
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| Source note | uspto-grants-2009_09 |
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