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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1182092생성일: 2026년 10월 27일

Imidazole → Benzyl (S)-3-(Boc-amino)-4-iodobutanoate

https://huagongshe.com/reaction/1182092

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물IodineHCID 807—
반응물TriphenylphosphineHCID 11776—
반응물Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoateHCID 10040985—
용매DichloromethaneHCID 6344—
생성물Benzyl (S)-3-(Boc-amino)-4-iodobutanoateHCID 11258642—

반응 단계

A suspension of polymer bound triphenyl phosphine (18.25 g, 54.76 mmol) in DCM (100 ml) is treated with iodine (12.2 g, 48.1 mmol) and the reaction mixture stirred at ambient temperature for 15 minutes. Imidazole (3.72 g, 54.7 mmol) is added and the reaction mixture stirred for a further 15 minutes. A solution of (S)-3-tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester (6.76 g, 21.9 mmol) in DCM (100 ml) is added. The suspension is stirred at reflux for 1.5 hours, then filtered through Celite™ filter material, washing through with DCM. The combined organic phase is washed with an aqueous solution of 10% sodium thiosulphate, water and brine, then dried over magnesium sulphate and evaporated. The crude product is chromatographed over flash silica using 8% ethylacetate in iso-hexane as eluent to afford (S)-3-tert-butoxycarbonylamino-4-iodo-butyric acid benzyl ester. [M-BOC] 320.12

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07288537B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-03e7a4abcdd845eca11b0eb3e0bc38af
출처 메모uspto-grants-2007_10