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HRID 376110作成日:2026年10月27日

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

https://huagongshe.com/reaction/376110

反応式

関与物質

役割名称HCID仕込み量
反応物1,5-HexadieneHCID 11598—
反応物Thionyl bromideHCID 68176—
反応物8-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-octanoic acid methyl esterHCID 21692618—
溶媒TetrahydrofuranHCID 8028—
生成物8-(N-benzyloxycarbonylamino)-4-bromomethyl-2-formylamino-oct-3-enoic acid methyl esterHCID 54439367—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05488140
出典データセットuspto-grants-1996_01
ORD IDord-29b9f6f387b844648778b9d2f6a3b458
出典メモuspto-grants-1996_01