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HRID 133844作成日:2026年10月27日

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

https://huagongshe.com/reaction/133844

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物beta-Phenylisovaleric acidHCID 13890—
反応物2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
反応物Lithium diisopropylamideHCID 2724682—
反応物Acetone cardiceHCID 18522661—
溶媒TetrahydrofuranHCID 8028—
生成物2-Ethyl-3-methyl-3-phenylbutanoic acidHCID 1127576430%

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390910B2
出典データセットuspto-grants-2008_06
ORD IDord-169b938c99dd42ff95790050937bc2a3
出典メモuspto-grants-2008_06