HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731014Generated: October 29, 2026
Water → 1-Chloro-2-(2,4-difluorophenyl)-3-pivaloyloxybutan-2-ol
https://huagongshe.com/reaction/731014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 86606435 | HCID 86606435 | — |
| Reactant | HCID 178505836 | HCID 178505836 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Chloro-2-(2,4-difluorophenyl)-3-pivaloyloxybutan-2-ol | HCID 23117041 | 60% |
Reaction Steps
A solution of 0.41 g (2.0 mmol) of (R)-1-chloro-3-pivaloyloxybutan-2-one in 5 mL of toluene was cooled to −20° C., and 3.2 mL (2.2 mmol) of a 0.69 M solution of 2,4-difluorophenylmagnesium bromide prepared by the same method as that in Example 3 was added dropwise thereto over a period of 5 minutes. After the completion of the dropwise addition, stirring was continued for another 1 hour, and 10 mL of a saturated aqueous solution of ammonium chloride was added to stop the reaction. Furthermore, 10 mL of water was added, and extraction was performed with ethyl acetate (20 mL×2). After drying over anhydrous sodium sulfate, concentration was performed under reduced pressure to obtain a crude product. A quantitative analysis was performed by HPLC. Thereby, the title compound was obtained in a yield of 60% ((2S,3R)/(2R,3R)=94/6 (the diastereomeric ratio was measured by HPLC under the same HPLC measurement conditions as those in Example 19)).
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-1d9192f2fdc340e08cdc399e44b4f4b2 |
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| Source note | uspto-grants-2009_09 |
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