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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1276488생성일: 2026년 10월 27일

Iodide Ion → 1-(Benzenesulfonyl)-3-(SR)-iodomethyl-4-(SR)-phenylpyrrolidine

https://huagongshe.com/reaction/1276488

반응식

참여 물질

역할이름HCID투입량
반응물Iodide IonHCID 30165—
반응물1-(Benzenesulfonyl)-3-(SR)-benzenesulfonyloxymethyl-4-(SR)-phenylpyrrolidineHCID 86756154—
용매AcetoneHCID 180—
생성물1-(Benzenesulfonyl)-3-(SR)-iodomethyl-4-(SR)-phenylpyrrolidineHCID 7020047796.8%

반응 단계

A solution of 234 mg (0.51 mmol) of 1-(benzenesulfonyl)-3-(SR)-benzenesulfonyloxymethyl-4-(SR)-phenylpyrrolidine (from Example 1, Step D) and 1.1 g (7.7 mmol) of sodiuim iodide in 8 mL of acetone was heated at reflux for 20 h. The reaction mixture was partitioned between 50 mL of ether and 30 mL of H2O and the layers were separated. The organic layer was washed with 30 mL of sat'd NaCl and dried over MgSO4. The aqueous layers were combined and extracted with 30 mL of ether. The extract was dried; the organic layers were combined. and concentrated in vacuo. Flash chromatography on 25 g of silica gel using 3:2 v/v hexanes/ether as the eluant afforded 211 mg (96%) of the title compound as an oil. 1H NMR (500 MHz, CDCl3): δ2.43 (t, J=9.8, 1H), 2.64-2.74 (m, 2H), 3.30 (dd, J=2.5, 7.8, 1H), 3.47 (q, J=6.7, 1H), 3.67-3.74 (3H), 7.05-7.95 (1OH). Mass Spectrum (NH3-CI): m/z 428 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06166037
출처 데이터셋uspto-grants-2000_12
ORD IDord-f466bd1aaae843c6860178b53a2e8d4d
출처 메모uspto-grants-2000_12