HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10923Generated: October 25, 2026
Water → (2R)-chloro-3-phenylpropionic acid
https://huagongshe.com/reaction/10923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Phenyllactic acid, (S)- | HCID 444718 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2R)-chloro-3-phenylpropionic acid | HCID 11458104 | 90.1% |
Reaction Steps
Thionyl chloride (0.66 ml, 9.0 mmol) was added dropwise to a solution of (2S)-2-hydroxy-3-phenylpropionic acid (500 mg, 3.0 mmol, optical purity 100% ee (S)) in 5 ml of tetrahydrofuran at room temperature, and the mixture was stirred for 15 hours. To the reaction mixture was added 170 mg (0.60 mmol) of tetra-n-butylammonium chloride, and the mixture was heated at 40° C. for 4 hours. Water (5 ml) was added to the reaction mixture and, after 30 minutes of stirring, the mixture was extracted with 90 ml of ethyl acetate. The organic phase was washed with 10 ml of a saturated aqueous solution of sodium chloride and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to give 499 mg (yield 90%) of the desired (2R)-chloro-3-phenylpropionic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094926B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-f826208111eb48df98d017f97031333a |
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| Source note | uspto-grants-2006_08 |
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