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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2238399생성일: 2026년 10월 27일

N-bromobutanimide → Methyl 2-[(tert-butoxycarbonyl)amino]-1-bromo-6-naphthoate

https://huagongshe.com/reaction/2238399

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물Methyl 6-[(tert-butoxycarbonyl)amino]-2-naphthoateHCID 44549532—
용매AcetonitrileHCID 6342—
생성물Methyl 2-[(tert-butoxycarbonyl)amino]-1-bromo-6-naphthoateHCID 4454991991%

반응 단계

A mixture of ester 147 (977 mg, 3.24 mmol) and NBS (664 mg, 3.73 mmol) in CH3CN (25 mL) was stirred at reflux for 45 min, then concentrated under reduced pressure. The residue was dissolved in CH2Cl2 and the solution was washed with 10% aqueous Na2SO3 and water (×2), dried, and concentrated under reduced pressure. The residue was purified by chromatography on silica gel, eluting with CH2Cl2, to give methyl 2-[(tert-butoxycarbonyl)amino]-1-bromo-6-naphthoate (148) (1.12 g, 91%) as a white solid: mp (petroleum ether) 130-131° C.; 1H NMR [(CD3)2SO] δ 8.93 (s, 1H), 8.65 (d, J=1.6 Hz, 1H), 8.64 (d, J=8.9 Hz, 1H), 8.16 (d, J=8.9 Hz, 1H), 8.11 (dd, J=8.9, 1.7 Hz, 1H), 7.86 (d, J=8.9 Hz, 1H), 3.93 (s, 3H), 1.50 (s, 9H). Anal. (C17H18BrNO4) C, H, N, Br.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07718688B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-303824f700934af7a3f54a2518379247
출처 메모uspto-grants-2010_05