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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1799209생성일: 2026년 10월 26일

Hydrochloric Acid → (4R)-4-(4-chloro-3-iodophenyl)pyrrolidin-2-one

https://huagongshe.com/reaction/1799209

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium IodideHCID 4875—
반응물Sodium NitriteHCID 23668193—
반응물(4R)-4-(3-amino-4-chlorophenyl)pyrrolidin-2-oneHCID 66724932—
용매WaterHCID 962—
용매Isopropanol methylene chlorideHCID 21966342—
생성물(4R)-4-(4-chloro-3-iodophenyl)pyrrolidin-2-oneHCID 66725090113.6%

반응 단계

To (4R)-4-(3-Amino-4-chlorophenyl)pyrrolidin-2-one (10 g, 47.62 mmol) was added a mixture of 12N HCl (30 mL) and ice cold water (20 mL) and cooled in ice. Sodium nitrite (3.7 g, 52.4 mmol) in 20 mL water was added dropwise. The mixture was stirred for 30 minutes. Potassium iodide (67.5 g, 404.8 mmol) in 100 mL of water was added dropwise at 0° C. The mixture was stirred for 1 h at 0° C. and then for 45 min at room temperature. One-hundred (100) mL of 20% IPA/DCM was added. The organic phase was separated and washed with 10% sodium thiosulfate, followed by water and brine. The combined organic layers were then evaporated in vacuo to give a reddish yellow oil, which was purified by silica gel chromatography (biotage) eluting with methylene chloride/methanol to provide 17.4 g (75% yield) of (4R)-4-(4-chloro-3-iodophenyl)pyrrolidin-2-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08344028B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-15c4235dcb624e6786b153f8faff6216
출처 메모uspto-grants-2013_01