HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032983Generated: October 25, 2026
Hydrochloric Acid → benzhydryl (2R)-hydroxy-4-phenylbutyrate
https://huagongshe.com/reaction/1032983
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 1,1'-(Diazomethylene)bis(benzene) | HCID 61230 | — |
| Reactant | Ethyl (R)-2-hydroxy-4-phenylbutyrate | HCID 2733848 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | benzhydryl (2R)-hydroxy-4-phenylbutyrate | HCID 54145254 | 38.4% |
Reaction Steps
Dissolve (R)-2-hydroxy-4-phenylbutyric acid, ethyl ester (4.16 g, 20 mmol) in methanol (40 mL). Add 1N lithium hydroxide (25 mL, 25 mmol) and stir under an atmosphere of argon for 3.5 hours. Acidify with 1N hydrochloric acid (25 mL), saturate with sodium chloride and extract with ethyl acetate (3×25mL). Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Take up the residue in methylene chloride (20 mL) and add diphenyldiazomethane (3.36 g, 17.3 mmol). Stir overnight and wash with saturated sodium hydrogen carbonate (2X). Dry (MgSO4), evaporate the solvent in vacuo and recrystallize (methylene chloride/hexane then again with cyclohexane) to give (R)-2-hydroxy-4-phenylbutyric acid, diphenylmethyl ester as white needles (2.3 g, 38%); mp 82°-84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05308841 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-6ee2a9f2f73749b68e9f44a751fe5e7a |
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| Source note | uspto-grants-1994_05 |
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