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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130520생성일: 2026년 10월 25일

Iodine → 1-Benzyl-4-(2-methyl-pentyl)-pyrrolidin-2-one

https://huagongshe.com/reaction/130520

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물2-BromopentaneHCID 7890—
반응물MagnesiumHCID 5462224—
반응물1-Benzyl-4-iodomethyl-pyrrolidin-2-oneHCID 12827276—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-4-(2-methyl-pentyl)-pyrrolidin-2-oneHCID 2188823369%

반응 단계

To a suspension of magnesium turnings (0.50 g, 0.021 mol) in 15 mL of dry THF under nitrogen, was added an iodine crystal and 2-bromopentane (2.88 g, 0.019 mol). After an exothermic reaction which was periodically cooled in an ice bath, the reaction was stirred at room temperature for 2 hours. Eight milliliters of Li2CuCl4 (made from 84 mg LiCl and 134 mg CuCl2 in 10 mL of dry THF) was added at 0° C. followed by dropwise addition of 1-Benzyl-4-iodomethyl-pyrolidine-2-one 75 in 15 mL dry THF, and the resulting suspension was let stir at 0° C. for 3 hours. Stirring was continued at room temperature for 1 hour before quenching with a saturated solution of ammonium chloride. Water was added to dissolve the precipitate formed, and the solution was then extracted with ether and dried over magnesium sulfate. The solvent was evaporated under vacuum and the residue chromatographed on silica eluting with 1:1 acetone/hexane to give 1.13 g, 69% of the 1-benzyl-4-(2-methyl-pentyl)-pyrrolidin-2-one 76. 1H NMR (CDCl3) δ 7.30 (m, 5H), 4.44 (m, 2H), 3.32 (m, 1H), 2.86 (m, 1H), 2.56 (m, 1H), 2.40 (m, 1H), 2.10 (m, 1H), 1.30 (m, 6H), 1.10 (m, 1H), 0.90 (m, 6H). MS, m/z (relative intensity): 261 [M+2H, 100%], 301 [M−H+CH3CN, 82%], 260 [M+H, 72%].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381747B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-d63168ab4abf447d88c381d7be11c418
출처 메모uspto-grants-2008_06