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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376110생성일: 2026년 10월 26일

1,5-Hexadiene → 8-(N-benzyloxycarbonylamino)-4-bromomethyl-2-formylamino-oct-3-enoic acid methyl ester

https://huagongshe.com/reaction/376110

반응식

참여 물질

역할이름HCID투입량
반응물1,5-HexadieneHCID 11598—
반응물Thionyl bromideHCID 68176—
반응물8-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-octanoic acid methyl esterHCID 21692618—
용매TetrahydrofuranHCID 8028—
생성물8-(N-benzyloxycarbonylamino)-4-bromomethyl-2-formylamino-oct-3-enoic acid methyl esterHCID 54439367—

반응 단계

To 2.46 g (6.5 mmol) of 8-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-octanoic acid methyl ester in 25 ml of tetrahydrofuran there are added 5.5 ml (46 mmol) of hexa-1,5-diene and then, dropwise at -50°, 2.6 ml (32.5 mmol) of thionyl bromide. The mixture is stirred at from 0° to 5° for 2 hours, poured into 25 ml of ice-cold saturated sodium hydrogen carbonate solution and extracted twice with 20 ml of methylene chloride each time. The organic phase is washed with 10 ml of saturated sodium chloride solution, dried over magnesium sulfate and concentrated to dryness by evaporation. The resulting oil is purified by chromatography on silica gel with hexane/ethyl acetate (3:1). 8-(N-benzyloxycarbonylamino)-4-bromomethyl-2-formylamino-oct-3-enoic acid methyl ester is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05488140
출처 데이터셋uspto-grants-1996_01
ORD IDord-29b9f6f387b844648778b9d2f6a3b458
출처 메모uspto-grants-1996_01