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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
Reactant1,1'-(Diazomethylene)bis(benzene)HCID 61230—
ReactantEthyl (R)-2-hydroxy-4-phenylbutyrateHCID 2733848—
SolventMethanolHCID 887—
Productbenzhydryl (2R)-hydroxy-4-phenylbutyrateHCID 5414525438.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308841
Source datasetuspto-grants-1994_05
ORD IDord-6ee2a9f2f73749b68e9f44a751fe5e7a
Source noteuspto-grants-1994_05