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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1159464생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1159464

반응식

참여 물질

역할이름HCID투입량
반응물(Iodomethyl)cyclopentaneHCID 2762531—
반응물Methyl 2-(4-(methylsulfonyl)phenyl)acetateHCID 16640928—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매MethidathionHCID 13709—
생성물Methyl 3-cyclopentyl-2-(4-methylsulfonylphenyl)propionateHCID 19261331—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07812167B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-d8ef0e9e40c04f8c93c5fde6d48cf5da
출처 메모uspto-grants-2010_10