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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353399Generated: October 29, 2026

Citric Acid → (r)-2-[2-(Tert-butoxy)-2-oxoethyl]-5-(2-methyl-1,1'-biphenyl-4-yl)-pentanoic acid (s)-alpha-methylbenzylamine salt

https://huagongshe.com/reaction/353399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant1-Phenethylamine, (-)-HCID 75818—
Reactant(R)-2-[2-(tert-butoxy)-2-oxoethyl]-5-(2-methyl-1,1'-biphenyl-4-yl)-pentanoic acidHCID 11825126—
ReactantHCID 69679961HCID 69679961—
SolventEthyl AcetateHCID 8857—
Product(r)-2-[2-(Tert-butoxy)-2-oxoethyl]-5-(2-methyl-1,1'-biphenyl-4-yl)-pentanoic acid (s)-alpha-methylbenzylamine saltHCID 8658520791%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

(R)-2-[2-(tert-butoxy)-2-oxoethyl]-5-(2-methyl-1,1′-biphenyl-4-yl)-pentanoic acid can be enantiomerically upgraded as the (S)-alpha-methylbenzylamine salt. Thus, (R)-2-[2-(tert-butoxy)-2-oxoethyl]-5-(2-methyl-1,1′-biphenyl-4-yl)-pentanoic acid cyclohexylamine salt (50 g, 0.10 mol, enantiomeric excess=72%) was partitioned between ethyl acetate (750 ml) and aqueous citric acid solution (10%, 750 ml). The organic phase was separated, washed with water (500 ml), then azeotropically dried by distillation at constant volume. (S)-alpha-methylbenzylamine (13.2 ml, 0.10 mol) was added dropwise over 5 min at 40° C., the mixture was allowed to cool to 20-25° C., and was then stirred for 24 hours. The mixture was filtered and the residue was washed with ethyl acetate (100 ml) and then dried in vacuo) at 45° C. for 2 hours to leave the title compound as a colourless solid (41.0 g, 91% yield, enantiomeric excess=96.4%, 95% pure by NMR).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750363B2
Source datasetuspto-grants-2004_06
ORD IDord-a2d79fee135c4c0a9eb639755ae74ff2
Source noteuspto-grants-2004_06