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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133844Generated: October 26, 2026

Iodoethane → 2-Ethyl-3-methyl-3-phenylbutanoic acid

https://huagongshe.com/reaction/133844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactantbeta-Phenylisovaleric acidHCID 13890—
Reactant2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ReactantLithium diisopropylamideHCID 2724682—
ReactantAcetone cardiceHCID 18522661—
SolventTetrahydrofuranHCID 8028—
Product2-Ethyl-3-methyl-3-phenylbutanoic acidHCID 1127576430%

Reaction Steps

In accordance with a modified literature procedure (Pfeffer, P. E.; Silbert, L. S.; Chirinko, J. M. J. Org. Chem. 37(3), 1972, 451-458), a solution of 3,3-dimethyl-3-phenyl propionic acid (0.47 g, 2.6 mmol, from Reference Example 22) in tetrahydrofuran (4.5 mL) is cooled to −40° C. (dry ice/acetone) while stirring under a nitrogen atmosphere. Lithium diisopropylamide (Aldrich, 2.0 M solution in tetrahydrofuran/ethylbenzene/heptane, 2.9 mL, 5.8 mmol) is added dropwise via syringe, followed by 1,3-dimethyl-3,4,5,6-tetrahydro-2(1 H)-pyrimidinone (DMPU, 0.35 mL, 2.9 mmol). The reaction mixture is then allowed to warm to room temperature and to stir for 30 minutes before being re-cooled to 0° C. (ice water bath). Ethyl iodide (0.31 mL, 3.9 mmol) is then added neat via syringe and the reaction mixture is allowed to stir overnight while warming to room temperature. The reaction is quenched by the addition of 10% aqueous hydrochloric acid solution and extracted thrice with ethyl acetate. The combined extracts are washed twice with 10% aqueous hydrochloric acid solution and once with saturated sodium chloride solution, dried over anhydrous sodium sulfite, and concentrated under reduced pressure. The crude solid is recrystallized from hexanes to afford pure material as a white solid (0.16 g, 30%). MS (ES−): (M−H)=205.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390910B2
Source datasetuspto-grants-2008_06
ORD IDord-169b938c99dd42ff95790050937bc2a3
Source noteuspto-grants-2008_06