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HRID 1159464作成日:2026年10月27日

(Iodomethyl)cyclopentane → Methyl 3-cyclopentyl-2-(4-methylsulfonylphenyl)propionate

https://huagongshe.com/reaction/1159464

反応式

関与物質

役割名称HCID仕込み量
反応物(Iodomethyl)cyclopentaneHCID 2762531—
反応物Methyl 2-(4-(methylsulfonyl)phenyl)acetateHCID 16640928—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒MethidathionHCID 13709—
生成物Methyl 3-cyclopentyl-2-(4-methylsulfonylphenyl)propionateHCID 19261331—

反応手順

To a solution of diispropylamine (25 mmol, 3.6 mL) in 24 mL of THF and 7.5 mL of methidathion (DMTP) at −78° C. is added n-BuLi (25 mmol, 10 mL, 2.5 M in hexanes) and the mixture stirred for 15 min. 4-Methylsulfonylphenylacetic acid methyl ester (24 mmol, 5.47 g) in 24 mL of THF and 7.5 mL of DMTP is then added dropwise over 30 min and the reaction is stirred for 90 min further. Cyclopentylmethyliodide (28.9 mmol, 6.08 g) in 10 mL of THF is then added dropwise and the reaction is stirred for 1 h at −78° C. before allowing to warm to RT. After 12 h, the reaction is quenched with water, evaporated and then partitioned between ethyl acetate (EtOAc) and brine, and the organic solution is dried and evaporated to afford an oil. The crude material is chromatographed on silica (eluent: 5%→25% EtOAc in hexanes) to afford 3-cyclopentyl-2-(4-methanesulfonyl-phenyl)-propionic acid methyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07812167B2
出典データセットuspto-grants-2010_10
ORD IDord-d8ef0e9e40c04f8c93c5fde6d48cf5da
出典メモuspto-grants-2010_10