HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730998Generated: October 25, 2026
Water → 1-Chloro-2-(2,4-difluorophenyl)-3-(tert-butyldimethylsilyloxy)butan-2-ol
https://huagongshe.com/reaction/730998
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (3R)-3-{[tert-Butyl(dimethyl)silyl]oxy}-1-chlorobutan-2-one | HCID 71415958 | — |
| Reactant | HCID 178505836 | HCID 178505836 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Chloro-2-(2,4-difluorophenyl)-3-(tert-butyldimethylsilyloxy)butan-2-ol | HCID 23117047 | 94% |
Reaction Steps
A solution of 0.69 g (3.0 mmol) of (R)-1-chloro-3-(tert-butyldimethylsilyloxy)butan-2-one in 5 mL of toluene was cooled to 0° C., and 5.3 mL (3.3 mmol) of a solution of 2,4-difluorophenylmagnesium bromide prepared by the same method as that in Example 3 was added dropwise over a period of 15 minutes. After the completion of the dropwise addition, stirring was continued for another 2 hours, and then 10 mL of a saturated aqueous solution of ammonium chloride was added to stop the reaction. Furthermore, 10 mL of water was added thereto, 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 colorless oil. A quantitative analysis was performed by HPLC (under the same HPLC measurement conditions as those in Example 3). Thereby, the title compound was obtained in a yield of 94% ((2S,3R): (2R,3R)=90:10).
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-fec31deb4ebe4b3e88dacc7d16a04cdb |
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| Source note | uspto-grants-2009_09 |
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