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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 470177생성일: 2026년 10월 25일

Iodine → (3aR,6aR)-5-iodo-2,2-dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one

https://huagongshe.com/reaction/470177

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물WaterHCID 962—
반응물PyridineHCID 1049—
반응물2,2-dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-oneHCID 13700992—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물(3aR,6aR)-5-iodo-2,2-dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-oneHCID 15236394—

반응 단계

3aR,6aR)-2,2-dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one (5-1) (1.2 g, 7.8 mmol, 1 equiv) was dissolved in DCM (50 mL) and pyridine (0.9 mL, 10.9 mmol, 1.4 equiv) was added followed by a solution of iodine (3.4 g, 13.2 mmol, 1.7 equiv) in THF (6 mL). The resulting mixture stirred overnight at ambient temperature. Upon disappearance of starting material, the reaction mixture was poured over water (30 mL), extracted with CHCl3 (3×50 mL), dried over MgSO4, filtered and concentrated. The crude residue was purified by flash chromatography (80 g SiO2, 0-40% EtOAc in hexanes) to yield (3aR,6aR)-5-iodo-2,2-dimethyl-3aH-cyclopenta[d][1,3]dioxol-4(6aH)-one (5-2) as a pale yellow solid. 1H NMR (500 MHz, CDCl3): δ 7.97 (d, J=2.5 Hz, 1H); 5.22 (dd, J=5.5, 2.5 Hz, 1H); 4.53 (d, J=5.5 Hz, 1H); 1.42 (s, 3H); 1.39 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629275B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-35540e3064fd404eae55ba65e82ba561
출처 메모uspto-grants-2014_01